48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome (Q24608052)

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English	48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome	scientific article

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48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome (English)

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Nicole Tartaglia

object named as

Nicole Tartaglia

1

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object named as

Philip Zeitler

5

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author name string

Natalie Ayari

2

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Susan Howell

3

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Cheryl D'Epagnier

4

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language of work or name

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publication date

June 2011

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Acta Paediatrica

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100

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6

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851-60

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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=3314712

7 April 2017

Dysregulation of X-linked gene expression in Klinefelter's syndrome and association with verbal cognition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

7 April 2017

Klinefelter syndrome and other sex chromosomal aneuploidies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

7 April 2017

Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

7 April 2017

Parental origin of the extra chromosomes in polysomy X

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

7 April 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=3314712

7 April 2017

X-chromosome polysomy in the male. The Leuven experience 1966-1987

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Tremor in 48,XXYY syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Reproduction in men with Klinefelter syndrome: the past, the present, and the future

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

New concepts in Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Testicular function in Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Endodontic treatment in three taurodontic teeth associated with 48,XXXY Klinefelter syndrome: a review and case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 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=3314712

27 September 2017

Endocrine function in a 48,XXYY adult with type 2 diabetes: case report with 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=3314712

27 September 2017

Klinefelter syndrome in clinical practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Male pubertal development and the role of androgen therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Cancer incidence and mortality in men with Klinefelter syndrome: a cohort study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Klinefelter's syndrome (XXY) as a genetic model for psychotic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

X-chromosome inactivation patterns and androgen receptor functionality influence phenotype and social characteristics as well as pharmacogenetics of testosterone therapy in Klinefelter patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

49,XXXXY: a distinct phenotype. Three new cases and review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

The psychoeducational profile of boys with Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Testosterone treatment of an XXYY male presenting with aggression: a case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

49,XXXXY syndrome: behavioural and developmental profiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

27 September 2017

An XXYY male with schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

30 May 2018

X-chromosome polysomy in the male

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Clinical findings and phenotype in a toddler with 48,XXYY syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism, and Increased Excretion of Follicle-Stimulating Hormone1

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Autism spectrum disorder and Klinefelter syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Olanzapine for violent schizophrenia and Klinefelter syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Is there an influence of X-chromosomal imprinting on the phenotype in Klinefelter syndrome? A clinical and molecular genetic study of 61 cases.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

X Chromosomal effects on social cognitive processing and emotion regulation: A study with Klinefelter men (47,XXY).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Cognitive and motor development during childhood in boys with Klinefelter syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

XXY (Klinefelter syndrome): a pediatric quantitative brain magnetic resonance imaging case-control study.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

The structural brain correlates of cognitive deficits in adults with Klinefelter's syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Update in andrology

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

A simple screening method for detection of Klinefelter syndrome and other X-chromosome aneuploidies based on copy number of the androgen receptor gene.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2011.02235.X

21 January 2018

Clinical variability and novel neurodevelopmental 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=3314712

28 November 2018

Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3314712

28 November 2018

A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the 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=3314712

28 November 2018

Klinefelter's syndrome (karyotype 47,XXY) and schizophrenia-spectrum pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rheumatic diseases and Klinefelter's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two 48,XXYY patients: clinical, cytogenetic and molecular aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 48,XXYY syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromosomes and psychosis. The case for a pseudoautosomal locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental origin of sex chromosome polysomies

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

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/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Androgen replacement in a 48, XXYY-male patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TWO CASES OF (PREPUBERTAL) KLINEFELTER'S SYNDROME WITH XXYY SEX CHROMOSOMES

1 reference

https://pubmed.ncbi.nlm.nih.gov/21342258

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1651-2227.2011.02235.X

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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