(Q35196836)

7 August 2017

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth (English)

1 reference

7 August 2017

Henke A

1

1 reference

7 August 2017

Wapenaar M

2

1 reference

7 August 2017

van Ommen GJ

3

1 reference

7 August 2017

Maraschio P

4

1 reference

7 August 2017

Camerino G

5

1 reference

7 August 2017

Rappold G

6

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

49

1 reference

7 August 2017

811-819

1 reference

7 August 2017

4

1 reference

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

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

The role of Yp in sex determination: new evidence from X/Y translocations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

The sex-determining region of the human Y chromosome encodes a finger protein.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Physical mapping of genes and sequences at the end of the human X chromosome short arm.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Fine mapping of the distal short arm of the human X chromosome using X/Y translocations.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

A physical map of the human pseudoautosomal region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

A long range restriction map of the pseudoautosomal region by partial digest PFGE analysis from the telomere

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Absence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

CpG-rich islands and the function of DNA methylation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Isolation and characterization of cell hybrids containing human Xp-chromosome fragments

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Localization of the human GM-CSF receptor gene to the X-Y pseudoautosomal region.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Y to X translocation in man

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Partial short arm deletions of the X chromosome and spontaneous pubertal development in girls with short stature

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683157

Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

13 July 2018

1 reference

12 December 2020

A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion

1 reference

12 December 2020

Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes

1 reference

12 December 2020

Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes

1 reference

12 December 2020

An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature

1 reference

12 December 2020

Identifiers

PMCID

1683157

1 reference

7 August 2017

1 reference