Prevalence of the fragile X syndrome in African-Americans (Q46936622)

26 December 2017

title

Prevalence of the fragile X syndrome in African-Americans (English)

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26 December 2017

Marshalyn Yeargin-Allsopp

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9

object named as

Marshalyn Yeargin-Allsopp

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26 December 2017

1

Dana C Crawford

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26 December 2017

author name string

Kellen L Meadows

2

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26 December 2017

James L Newman

3

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26 December 2017

Lisa F Taft

4

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26 December 2017

Elizabeth Scott

5

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26 December 2017

Mary Leslie

6

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26 December 2017

Lisa Shubek

7

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26 December 2017

Patricia Holmgreen

8

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Coleen Boyle

10

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Stephanie L Sherman

11

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publication date

1 July 2002

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26 December 2017

American Journal of Medical Genetics Part A

published in

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26 December 2017

volume

110

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page(s)

226-233

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issue

3

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26 December 2017

Molecular-neurobehavioral associations in females with the fragile X full mutation.

cites work

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https://api.crossref.org/works/10.1002%2FAJMG.10427

FMR1 protein: conserved RNP family domains and selective RNA binding

21 January 2018

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Examination of factors associated with instability of the FMR1 CGG repeat.

21 January 2018

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Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10427

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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/10.1002%2FAJMG.10427

Physical characteristics of young boys with fragile X syndrome: reasons for difficulties in making a diagnosis in young males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Advances in research on the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Fragile X syndrome is less common than previously estimated

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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/10.1002%2FAJMG.10427

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Contribution of the FMR1 gene mutation to human intellectual dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Problems in the diagnosis of fragile X syndrome in young children are still present.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

DNA methylation represses FMR-1 transcription in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10427

FRAXA and FRAXE: the results of a five year survey

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10427

21 January 2018

Identifiers

DOI

10.1002/AJMG.10427

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26 December 2017

PubMed ID

12116230

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26 December 2017