Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition-Reference-Cited by-同舟云学术

Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition

Published:2009-10-21 Issue:3 Volume:18 Page:285-290
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Rio Marlène,Malan Valérie,Boissel Sarah,Toutain Annick,Royer Ghislaine,Gobin Stéphanie,Morichon-Delvallez Nicole,Turleau Catherine,Bonnefont Jean-Paul,Munnich Arnold,Vekemans Michel,Colleaux Laurence

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009159.pdf

Reference43 articles.

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3. Ropers HH : X-linked mental retardation: many genes for a complex disorder. Curr Opin Genet Dev 2006; 16: 260–269.

4. Chen W, Jensen LR, Gecz J et al: Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. Eur J Hum Genet 2007; 15: 375–378.

5. Raymond FL, Tarpey P : The genetics of mental retardation. Hum Mol Genet 2006; 15: R110–R116. Review.

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