335.4kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features-Reference-Cited by-同舟云学术

335.4kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features

Published:2012-09 Issue:2 Volume:505 Page:384-387
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Alesi Viola,Bertoli Marta,Barrano Giuseppe,Torres Barbara,Pusceddu Silvia,Pastorino Myriam,Perria Chiara,Nardone Anna Maria,Novelli Antonio,Serra Gigliola

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference20 articles.

1. Monogenic causes of X-linked mental retardation;Chelly;Nat. Rev. Genet.,2001

2. XLMR genes: update 2007;Chiurazzi;Eur. J. Hum. Genet.,2008

3. Phenotypic spectrum associated with duplication of Xp11.22–p11.23 includes autism spectrum disorder;Chung;Eur. J. Med. Genet.,2011

4. Microduplication of Xp11.23p11.3 with effects on cognition, behavior, and craniofacial development;El-Hattab;Clin. Genet.,2011

5. Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation;Freude;Am. J. Hum. Genet.,2004

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