(Q42591431)

3 November 2017

A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23 (English)

1 reference

premature ovarian failure

3 November 2017

1 reference

Amati P

1

1 reference

3 November 2017

Gasparini P

2

1 reference

3 November 2017

Zlotogora J

3

1 reference

3 November 2017

Zelante L

4

1 reference

3 November 2017

Chomel JC

5

1 reference

3 November 2017

Kitzis A

6

1 reference

3 November 2017

Kaplan J

7

1 reference

3 November 2017

Bonneau D

8

1 reference

3 November 2017

language of work or name

English

0 references

publication date

1 May 1996

1 reference

American Journal of Human Genetics

3 November 2017

1 reference

3 November 2017

58

1 reference

3 November 2017

5

1 reference

3 November 2017

1089-1092

1 reference

The genetics of XX gonadal dysgenesis

3 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

Blepharophimosis and its association with female infertility

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

The blepharophimosis, ptosis, and epicanthus inversus syndrome: delineation of two types

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome)

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

Activin/inhibin beta B subunit gene disruption leads to defects in eyelid development and female reproduction.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

Blepharophimosis syndrome is linked to chromosome 3q.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914611

Blepharophimosis, ptosis, epicanthus inversus, and primary amenorrhea. A dominant trait

16 August 2018

1 reference

12 December 2020

Familial Blepharophimosis: An Uncommon Marker of Ovarian Dysgenesis

1 reference

12 December 2020

Definition of the blepharophimosis, ptosis, epicanthus inversus syndrome critical region at chromosome 3q23 based on the analysis of chromosomal anomalies

1 reference

12 December 2020

A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23

1 reference

12 December 2020

Identifiers

1 reference

3 November 2017

PubMed publication ID

8651270

1 reference