A review of trisomy X (47,XXX) (Q21093168)

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English	A review of trisomy X (47,XXX)	scientific article

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scholarly article

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4 references

20 June 2019

30 June 2019

14 September 2019

24 November 2020

A review of trisomy X (47,XXX) (English)

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sex chromosome aberration

4 references

20 June 2019

30 June 2019

14 September 2019

24 November 2020

genetic variation

1 reference

14 September 2019

Nicole Tartaglia

object named as

Nicole R Tartaglia

1

author given names

Nicole R

author last names

Tartaglia

1 reference

Dimensions Publication ID

7 August 2022

author name string

Susan Howell

2

author given names

Susan

author last names

Howell

1 reference

Dimensions Publication ID

7 August 2022

Ashley Sutherland

3

author given names

Ashley

author last names

Sutherland

1 reference

Dimensions Publication ID

7 August 2022

Rebecca Wilson

4

author given names

Rebecca

author last names

Wilson

1 reference

Dimensions Publication ID

7 August 2022

Lennie Wilson

5

author given names

Lennie

author last names

Wilson

1 reference

Dimensions Publication ID

7 August 2022

language of work or name

0 references

publication date

11 May 2010

4 references

20 June 2019

30 June 2019

14 September 2019

24 November 2020

Orphanet Journal of Rare Diseases

4 references

20 June 2019

30 June 2019

14 September 2019

24 November 2020

5

0 references

1

0 references

8

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copyright license

Creative Commons Attribution 2.0 Generic

4 references

Europe PubMed Central

20 June 2019

Europe PubMed Central

30 June 2019

Europe PubMed Central

14 September 2019

Europe PubMed Central

24 November 2020

copyright status

0 references

A new look at XXYY syndrome: medical and psychological features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

19 March 2017

Xist and the order of silencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

19 March 2017

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

19 March 2017

Sex chromosome tetrasomy and pentasomy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

19 March 2017

Triple X syndrome: a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

The origin of human aneuploidy: where we have been, where we are going

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Evidence for the existence of the human "super female".

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

47,XXX in an adolescent with premature ovarian failure and autoimmune disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Life adaptation in 35 adults with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Neurobehavioral phenotype of Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Long-term outcome in children of sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Volumetric magnetic resonance imaging study of the brain in subjects with sex chromosome aneuploidies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Intelligence and achievement in children with extra X aneuploidy: a longitudinal perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Neuropsychological impairment in 42 adolescents with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Chromosome abnormalities and spontaneous fetal death following amniocentesis: further data and associations with maternal age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

Fertility in 47,XXX and 45,X patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

12 September 2017

X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

27 September 2017

Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

27 September 2017

The pseudoautosomal regions of the human sex chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

27 September 2017

A possible explanation for the low incidence of gonosomal aneuploidy among the offspring of triplo-X individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

27 September 2017

Genetic influences on learning disabilities and speech and language disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

27 September 2017

Brain magnetic resonance imaging findings in 49,XXXXY syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Sex chromosomal anomalies in pregnancies conceived through intracytoplasmic sperm injection: a case for genetic counselling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Triple mosaicism of X-chromosomes with bipolar affective psychosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Sex chromosomal aneuploidy: prospective and longitudinal studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Variability at the telomeres of the human X/Y pseudoautosomal region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Gross and fine motor development in 45,X and 47,XXX girls.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Verbal and spatial processing efficiency in 32 children with sex chromosome abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

47,XXX: what is the prognosis?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Intrauterine growth retardation and minor anomalies in 47,XXX children.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Summary of clinical findings in children and young adults with sex chromosome anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Sex chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Edinburgh study of growth and development of children with sex chromosome abnormalities. IV.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Prognosis of prenatally diagnosed children with sex chromosome aneuploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Abnormalities of the sex chromosomes: a prospective study on randomly identified newborns

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Autoimmunity in a patient with 47,XXX karyotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

30 May 2018

Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Partial epilepsy and 47,XXX karyotype: report of four cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Electroencephalographic and epileptic patterns in X chromosome anomalies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Head circumference and IQ of children with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Psychosocial adaptation of 39 adolescents with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Language and cognitive development in 47,XXX females followed since birth.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Learning disabilities in children with sex chromosome anomalies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Short communication: skeletal maturation of children with sex chromosome abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883963

29 November 2018

Triple-X syndrome and premature ovarian failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association between triple X and psychosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

True 47,XXX in a patient with premature ovarian failure: the first reported case in Thailand

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The growth of XXX females: population-based studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Longitudinal growth studies on children with sex chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Summary overview of behavioural development in individuals with neonatally identified X and Y aneuploidy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schizophrenia and sex chromosome anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tall stature as presenting symptom in a girl with triple X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Speech and language development in 41 children with sex chromosome anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20459843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1750-1172-5-8

1 reference

Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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