The Italian XLMR bank: a clinical and molecular database-Reference-Cited by-同舟云学术

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The Italian XLMR bank: a clinical and molecular database

Published:2007-01 Issue:1 Volume:28 Page:13-18
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Pescucci C.,Caselli R.,Mari F.,Speciale C.,Ariani F.,Bruttini M.,Sampieri K.,Mencarelli M.A.,Scala E.,Longo I.,Artuso R.,Renieri A.,Meloni I.,

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. Mental retardation in over half-a-million consecutive livebirths: an epidemiological study;Baird;Am J Ment Defic,1985

2. X chromosome array-CGH for the identification of novel X-linked mental retardation genes;Bauters;Eur J Med Genet,2005

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

4. Guidelines for genetic biobanks;Dagna Bricarelli;Analysis,2003

5. The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain;Gecz;Front Biosci,2004

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X‐linked microcephalic intellectual deficit;Clinical Genetics;2013-03

2. Mental retardation and Xq12–Xq23: candidate loci for nonspecific mental retardation in the male population of the QinBa region;Psychiatric Genetics;2009-02

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