(Q33595970)

28 July 2017

1 reference

title

Chromosomal localisation of a gene(s) for Turner stigmata on Yp. (English)

1 reference

28 July 2017

Ogata T

1

1 reference

28 July 2017

Tyler-Smith C

series ordinal

2

1 reference

28 July 2017

Purvis-Smith S

series ordinal

3

1 reference

28 July 2017

Turner G

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1993

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

30

1 reference

28 July 2017

918-922

1 reference

28 July 2017

11

1 reference

Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Neck web and congenital heart defects: a pathogenic association in 45 X-O Turner syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

A Y/5 translocation in a 45,X male with cri du chat syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Pathogenesis of congenital defects associated with Turner's syndrome: the role of hypoalbuminemia and edema

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Small deletions of the short arm of the Y chromosome in 46,XY females

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Breakage of the human Y-chromosome short arm between two blocks of tandemly repeated DNA sequences.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

A sterile male with 45,X0 and a Y;22 translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Chromosomal localisation of a pseudoautosomal growth gene(s)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Male with 45,X karyotype.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Sexual and somatic determinants of the human Y chromosome: studies in a 46,XYp- phenotypic female

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Lymphatic malformation in human fetuses. A study of fetuses with Turner's syndrome or status Bonnevie-Ullrich

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

Analysis of complex Y chromosome aberrations using a single DNA probe (Y-367).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016599

A new case of Y to X translocation in a female

30 October 2018

1 reference

12 December 2020

45,X constitution in a H-Y antigen positive boy with partial monosomy 5p

1 reference

12 December 2020

Turner syndrome resulting from partial deletion of Y chromosome short arm: localization of male determinants

1 reference

12 December 2020

Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11

1 reference

12 December 2020

Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe

1 reference

12 December 2020

Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome

1 reference

12 December 2020

Partial gonadal dysgenesis in a patient with a marker Y chromosome

1 reference

12 December 2020

Expression of RPS4X in fibroblasts from patients with structural aberrations of the X chromosome

1 reference

12 December 2020

Deletion mapping of H-Y antigen to the long arm of the human Y chromosome

1 reference

12 December 2020

The human Y chromosome: a 43-interval map based on naturally occurring deletions

1 reference

12 December 2020

Absence of Turner stigmata in a 46,XYp-female

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.30.11.918

1 reference

28 July 2017

1 reference

28 July 2017

1 reference