Fragile X syndrome: the FMR1 CGG repeat distribution among world populations (Q24629837)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A fragile balance: FMR1 expression levels

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

CGG repeat in the FMR1 gene: size matters

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Mechanisms of trinucleotide repeat instability during human development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A systematic review of population screening for fragile X syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Gene expression profiling identifies WNT7A as a possible candidate gene for decreased cancer risk in fragile X syndrome patients.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Examination of FMR1 transcript and protein levels among 74 premutation carriers

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A review of fragile X premutation disorders: expanding the psychiatric perspective

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

The nucleotide binding dynamics of human MSH2-MSH3 are lesion dependent

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Microsatellite repeat instability and neurological disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Inherited susceptibility to common cancers

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Fragile X syndrome in Korea: a case series and a review of the literature

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Reproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Features of trinucleotide repeat instability in vivo

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

ATR protects the genome against CGG.CCG-repeat expansion in Fragile X premutation mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Whole genome microarray analysis of gene expression in subjects with fragile X syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Elevated FMR1 mRNA in premutation carriers is due to increased transcription.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

DNA structures, repeat expansions and human hereditary disorders.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

The genetic basis of premature ovarian failure.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Transcription, translation and fragile X syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Acceptance of fragile X premutation genetic screening in women with ovarian dysfunction

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Social behavior deficits in the Fmr1 mutant mouse

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Long CGG-repeat tracts are toxic to human cells: implications for carriers of Fragile X premutation alleles

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

CTG repeat instability and size variation timing in DNA repair-deficient mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Sunrise at the synapse: the FMRP mRNP shaping the synaptic interface

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

FMR1 and the fragile X syndrome: human genome epidemiology review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

The female and the fragile X reviewed

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Genetic diversity at the FMR1 locus in the Indonesian population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

An assessment of screening strategies for fragile X syndrome in the UK.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

FRAXA and FRAXE: the results of a five year survey

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Prevalence and clinical characteristics of fragile X syndrome at child development clinic, Ramathibodi Hospital

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Familial transmission of the FMR1 CGG repeat.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Population studies of the fragile X: a molecular approach

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

DNA testing for fragile X syndrome in schools for learning difficulties

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Fragile X gene instability: anchoring AGGs and linked microsatellites

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

The frequency of the fragile X chromosome among schoolchildren in Coventry

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Association of FMR1 repeat size with ovarian dysfunction

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Molecular evidence that fragile X syndrome occurs in the South African black population

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

FMR1 in global populations

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A point mutation in the FMR-1 gene associated with fragile X mental retardation

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A population-based study on the causes of mild and severe mental retardation.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Evolution of the cryptic FMR1 CGG repeat

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Frequency of the fragile X syndrome in Japanese mentally retarded males.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Phylogenetic relations of humans and African apes from DNA sequences in the psi eta-globin region

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations.

30 May 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Prevalence of the fragile X syndrome in African-Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Haplotype and AGG interspersion analysis of FMR1 alleles in a Croatian population: no founder effect detected in patients with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Mosaicism for FMR1 and FMR2 deletion: a new case

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

DNA analysis of the fragile X syndrome in an at risk pediatric population in croatia: simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Protein composition of the intranuclear inclusions of FXTAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Characterization of the full fragile X syndrome mutation in fetal gametes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

FMR1 alleles in Tasmania: a screening study of the special educational needs population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Fragile X carrier screening and FMR1 allele distribution in the Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Molecular screening of FRAXA and FRAXE in Indian patients with unexplained mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Incidence of fragile X in 5,000 consecutive newborn males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Genetic diversity at the FMR1 locus in Mexican population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Molecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Prevalence of fra(X) in the county of Funen in Denmark is lower than expected.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Pilot fragile X screening in normal population of Taiwan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Evidence of early ovarian aging in fragile X premutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Paternal transmission of fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00694.X

Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Fragile x-syndrome: clinical and molecular studies.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

A clinical study of mentally retarded children with fragile X syndrome in Saudi Arabia.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Fragile X syndrome: a clinico-genetic study of mentally retarded patients in Kuwait.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Screening for fragile X syndrome: results from a school for mentally retarded children.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Stability of the FMR1 CGG repeat in a Basque sample.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

The prevalence of fragile-X syndrome in an institution for people with learning disability.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Molecular characterization of the fragile-X syndrome in the Mexican population.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

Striking founder effect for the fragile X syndrome in Finland.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288311

FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardation

28 November 2018

1 reference

12 December 2020

Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation

1 reference

12 December 2020

Evidence of founder chromosomes in fragile X syndrome

1 reference

12 December 2020

Strong founder effect for the fragile X syndrome in Sweden

1 reference

12 December 2020

Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India

1 reference

12 December 2020

Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity

1 reference

12 December 2020

Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases

1 reference

12 December 2020

Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus

1 reference

12 December 2020

Fragile X founder effect?

1 reference

12 December 2020

Prevalence of fragile X syndrome

1 reference

12 December 2020

Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males

1 reference

12 December 2020

Founder effect in a Belgian-Dutch fragile X population

1 reference

12 December 2020

1 reference

12 December 2020

Fragile X syndrome occurs in the South African black population

1 reference

12 December 2020

Preventive screening for the fragile X syndrome

1 reference

12 December 2020

Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico

1 reference

12 December 2020

Fully mutated and gray-zone FRAXA alleles in Brazilian mentally retarded boys

1 reference

12 December 2020

Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations

1 reference

12 December 2020

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene

1 reference

12 December 2020

Direct mutation analysis of 495 patients for fragile X carrier status/proband diagnosis

1 reference

12 December 2020

Studies of the fragile (X) syndrome in populations of mentally retarded individuals in Hawaii

1 reference

12 December 2020

A survey of fragile X syndrome in a sample from Spanish Basque country

1 reference

12 December 2020

Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR

1 reference

12 December 2020

DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population

1 reference

12 December 2020

Premature ovarian failure

1 reference

12 December 2020

10.1111/J.1469-1809.2011.00694.X

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

22188182

1 reference