(Q50533116)

English

Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndrome.

scientific article published on 16 February 2016

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scholarly article

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndrome. (English)

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

0 references

author name string

Faruk H Orge

1

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Suhail A Dar

2

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Christie N Blackburn

3

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Sarah J Grimes-Hodges

4

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Anna L Mitchell

5

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

publication date

16 February 2016

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Ophthalmic Genetics

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

37

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

3

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

323-327

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2015.1071407

21 January 2018

An autosomal dominant syndrome of renal and anogenital malformations with syndactyly.

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2015.1071407

21 January 2018

CDK10/cyclin M is a protein kinase that controls ETS2 degradation and is deficient in STAR syndrome

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2015.1071407

21 January 2018

An overview of isolated and syndromic oesophageal atresia

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2015.1071407

21 January 2018

The Townes-Brocks syndrome

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2015.1071407

21 January 2018

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2015.1071407

21 January 2018

Identifiers

10.3109/13816810.2015.1071407

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/26882209

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