(Q34297490)

1 August 2017

title

The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases (English)

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1 August 2017

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Chang HJ

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1 August 2017

Clark RD

series ordinal

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1 August 2017

Bachman H

series ordinal

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1 August 2017

language of work or name

English

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publication date

1 January 1990

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

156-167

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KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

European collaborative study on prenatal diagnosis: mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Monozygotic twins of different sex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

The 45XO/46XY mosaic intersex syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Intersex conditions masquerading as simple hypospadias

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Occurrence of tumors in dysgenetic gonads

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Gonadoblastoma. A review of 74 cases

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Sex chromoseme mosaicism in male pseudohermaphrodism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

45,X/46,XY mosaicism. A clinical review and report of ten cases

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

The age of occurrence of gonadal tumors in intersex patients with a Y chromosome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

The occurrence of gonadal dysgenesis in association with monozygotic twinning

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

6 July 2018

Mixed gonadal dysgenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

Monozygotic twins discordant for sex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

The relationship of neoplasia to disorders of abnormal sexual differentiation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683543

A clinical and cytogenetic study of fifteen patients with 45,X/46XY gonadal dysgenesis

6 July 2018

1 reference

12 December 2020

Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype

1 reference

12 December 2020

45,X/46,XY chromosome mosaicism detected by midtrimester amniocentesis in amniocyte clones

1 reference

12 December 2020

Presence of H-Y antigen in female patients with sex-chromosome mosaics and absence of testicular tissue

1 reference

12 December 2020

Cytogenetic and clinical findings in ten 45, X/46, XY patients*

1 reference

12 December 2020

Prenatal diagnosis of chromosome mosaicism

1 reference

12 December 2020

A Canadian collaborative study of mosaicism in amniotic fluid cell cultures

1 reference

12 December 2020

Cytogenetic diagnosis using midtrimester fetal blood samples: application to suspected mosaicism and other diagnostic problems

1 reference

12 December 2020

Carcinoma in situ of the testis in children with 45,X/46,XY gonadal dysgenesis

1 reference

12 December 2020

Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testes

1 reference

12 December 2020

A cytogenetic and endocrinologic study of a set of monozygotic isokaryotic 45,X/46,XY twins discordant for phenotypic sex: mosaicism versus chimerism

1 reference

12 December 2020

Phenotypic spectrum of 45,X/46,XY individuals

1 reference

12 December 2020

Prenatal diagnosis of 45,X/46,XY mosaicism in a fetus with asymmetric gonadal dysgenesis

1 reference

12 December 2020

XO-XY mosaicism in a phenotypic female with gonadoblastoma. Attempt of classification of the clinical picture of the XO-XY mosaics

1 reference

12 December 2020

Human intersex with chromosome mosaicism of type XY/XO. Report of a case

1 reference

12 December 2020

Gonadal dysgenesis and its unilateral variant with testis in monozygous twins: related to discordance in sex chromosomal status

1 reference

12 December 2020

Chromosomal mosaicism in amniotic fluid cell cultures

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12 December 2020

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

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12 December 2020

Identifiers

PMC publication ID

1683543

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1 August 2017

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