Analysis of X chromosome inactivation in autism spectrum disorders-Reference-Cited by-同舟云学术

Analysis of X chromosome inactivation in autism spectrum disorders

Published:2008-03-24 Issue:6 Volume:147B Page:830-835
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gong Xiaohong,Bacchelli Elena,Blasi Francesca,Toma Claudio,Betancur Catalina,Chaste Pauline,Delorme Richard,Durand Christelle M.,Fauchereau Fabien,Botros Hany Goubran,Leboyer Marion,Mouren-Simeoni Marie-Christine,Nygren Gudrun,Anckarsäter Henrik,Rastam Maria,Gillberg I. Carina,Gillberg Christopher,Moreno-De-Luca Daniel,Carone Simona,Nummela Ilona,Rossi Mari,Battaglia Agatino,Jarvela Irma,Maestrini Elena,Bourgeron Thomas,

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference27 articles.

1. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees;Abecasis;Nat Genet,2002

2. X chromosome-Inactivation patterns of 1,005 phenotypically unaffected females;Amos-Landgraf;Am J Hum Genet,2006

3. A genomewide screen for autism spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q 25-27;Auranen;Am J Hum Genet,2002

4. Mapping autism risk loci using genetic linkage and chromosomal rearrangements;Szatmari;Nat Genet,2007

5. Mutation analysis of the coding sequence of the MECP2 gene in infantile autism;Beyer;Hum Genet,2002

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