SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies. (Q52040037)

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scientific article published in October 2005

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Language	Label	Description	Also known as
English	SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.	scientific article published in October 2005

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

main subject

hearing loss

1 reference

based on heuristic

inferred from title

author name string

Stephanie A Hagstrom

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

Gayle J T Pauer

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

Janet Reid

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

Ellen Simpson

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

Sue Crowe

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

Irene H Maumenee

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

Elias I Traboulsi

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

language of work or name

English

0 references

publication date

1 October 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

published in

American Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

volume

138A

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

page(s)

95-98

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

cites work

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

stated in

Crossref

reference URL

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

retrieved

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.30803

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

PubMed publication ID

16145681

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16145681

retrieved

20 April 2018

reference URL

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

 

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