Filamin A mutation is one cause of FG syndrome-Reference-Cited by-同舟云学术

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Filamin A mutation is one cause of FG syndrome

Published:2007 Issue:16 Volume:143A Page:1876-1879
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Unger Sheila,Mainberger Anita,Spitz Christian,Bähr Anna,Zeschnigk Christine,Zabel Bernhard,Superti-Furga Andrea,Morris-Rosendahl Deborah J.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

1. The FG syndrome: Report of a large Italian series

2. A gene for FG syndrome maps in the Xq12-q21.31 region

3. Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome

4. Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?

5. FG syndrome: Linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]

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