The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment-Reference-Cited by-同舟云学术

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The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment

Published:2010-06-15 Issue:7 Volume:153B Page:1342-1346
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Cocchella Alessandro,Malacarne Michela,Forzano Francesca,Marciano Carmela,Pierluigi Mauro,Perroni Lucia,Faravelli Francesca,Di Maria Emilio

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.31107/fullpdf

Reference21 articles.

1. Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development;Bayatti;Eur J Neurosci,2008

2. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity;Buxbaum;Am J Hum Genet,2001

3. Association of the alpha4 integrin subunit gene (ITGA4) with autism;Correia;Am J Med Genet Part B,2009

4. Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3);Gallagher;J Autism Dev Disord,2003

5. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p;International Molecular Genetic Study of Autism Consortium (IMGSAC);Am J Hum Genet,2001

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3. Zinc in Cognitive Impairment and Aging;Biomolecules;2022-07-18

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