(Q52040037)

English

SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.

scientific article published in October 2005

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scholarly article

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies. (English)

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

1 reference

based on heuristic

inferred from title

author name string

Stephanie A Hagstrom

1

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

Gayle J T Pauer

2

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

Janet Reid

3

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

Ellen Simpson

4

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

Sue Crowe

5

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

Irene H Maumenee

6

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

Elias I Traboulsi

7

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

language of work or name

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publication date

1 October 2005

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

American Journal of Medical Genetics

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

138A

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

95-98

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

2

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

The gene for the embryonic stem cell coactivator UTF1 carries a regulatory element which selectively interacts with a complex composed of Oct-3/4 and Sox-2.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30803

21 January 2018

Identifiers

10.1002/AJMG.A.30803

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/16145681

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