An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome-Reference-Cited by-同舟云学术

An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome

Published:2005 Issue:3 Volume:139A Page:221-226
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Jehee Fernanda Sarquis,Rosenberg Carla,Krepischi-Santos Ana Cristina,Kok Fernando,Knijnenburg Jeroen,Froyen Guy,Vianna-Morgante Angela M.,Opitz John M.,Passos-Bueno Maria Rita

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. Accelerated Transcription of PRPS1 in X-linked Overactivity of Normal Human Phosphoribosylpyrophosphate Synthetase

2. X chromosome array-CGH for the identification of novel X-linked mental retardation genes

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

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

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