(Q36714782)

15 August 2017

0 references

Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports (English)

1 reference

15 August 2017

Xuefeng Gao

1

1 reference

15 August 2017

Guian Chen

2

1 reference

15 August 2017

Jing Huang

3

1 reference

15 August 2017

Quan Bai

4

1 reference

15 August 2017

Nan Zhao

5

1 reference

15 August 2017

Minjie Shao

6

1 reference

15 August 2017

Liping Jiao

7

1 reference

15 August 2017

Yanling Wei

8

1 reference

15 August 2017

Liang Chang

9

1 reference

15 August 2017

Dan Li

10

1 reference

15 August 2017

Liping Yang

11

1 reference

15 August 2017

3 February 2013

1 reference

Journal of Assisted Reproduction and Genetics

15 August 2017

1 reference

15 August 2017

30

1 reference

15 August 2017

3

1 reference

15 August 2017

431-435

1 reference

Localisation of the Y chromosome stature gene to a 700 kb interval in close proximity to the centromere

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Sox9 induces testis development in XX transgenic mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

XX males without SRY gene and with infertility

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

An SRY-negative XX male with Huriez syndrome.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Autosomal XX sex reversal caused by duplication of SOX9.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

True hermaphroditism with partial duplication of chromosome 22 and without SRY.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Analytic review: nature and origin of males with XX sex chromosomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Comparison of adult height between patients with XX and XY gonadal dysgenesis: support for a Y specific growth gene(s)

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Sex in the 90s: SRY and the switch to the male pathway

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Two SRY-negative XX male brothers without genital ambiguity

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

The role of the sex-determining region Y gene in the etiology of 46,XX maleness

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Clinical and molecular analysis of XX sex reversed patients.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3607678

SRY-negative 46,XX male with normal genitals, complete masculinization and infertility

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10815-013-9939-7

Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: Case report

21 January 2018

1 reference

12 December 2020

46,XX sex reversal with partial duplication of chromosome arm 22q

1 reference

12 December 2020

A possible common origin of "Y-negative" human XX males and XX true hermaphrodites

1 reference

12 December 2020

XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE

1 reference

12 December 2020

A 46,XX SRY-negative man with complete virilization and infertility as the main anomaly

1 reference

12 December 2020

An XX male with the sex-determining region Y gene inserted in the long arm of chromosome 16

1 reference

12 December 2020

10.1007/S10815-013-9939-7

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

23378127

1 reference