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Genotype–Phenotype Association Studies of Chromosome 8p Inverted Duplication Deletion Syndrome

Individuals diagnosed with chromosome 8p inverted duplication deletion (invdupdel(8p)) manifest a wide range of clinical features and cognitive impairment. The purpose of this study is to employ array CGH technology to define more precisely the cytogenetic breakpoints and regions of copy number vari...

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Detalhes bibliográficos
Publicado no:Behav Genet
Main Authors: Fisch, Gene S., Davis, Ryan, Youngblom, Janey, Gregg, Jeff
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4557779/
https://ncbi.nlm.nih.gov/pubmed/21259039
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-011-9447-4
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