Microduplications in an Autism Multiplex Family Narrow the Region of Susceptibility for Developmental Disorders on 15q24 and Implicate 7p21

Copy number variations (CNVs) play a crucial role in the intricate genetics of autism spectrum disorders. A region on chromosome 15q24 vulnerable to both deletions and duplications has been previously implicated in a range of phenotypes including autism, Asperger’s syndrome, delayed development, and...

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Pubblicato in:Am J Med Genet B Neuropsychiatr Genet
Autori principali: Cukier, Holly N., Salyakina, Daria, Blankstein, Sarah F., Robinson, Joycelyn L., Sacharow, Stephanie, Ma, Deqiong, Wright, Harry H., Abramson, Ruth K., Menon, Ramkumar, Williams, Scott M., Haines, Jonathan L., Cuccaro, Michael L., Gilbert, John R., Pericak-Vance, Margaret A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2011
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5490366/
https://ncbi.nlm.nih.gov/pubmed/21480499
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.31188
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