Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15‐16.1

BACKGROUND: During whole genome microarray‐based comparative genomic hybridisation (array CGH) screening of subjects with idiopathic intellectual disability, we identified two unrelated individuals with a similar de novo interstitial microdeletion at 2p15‐2p16.1. Both individuals share a similar cli...

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Detalhes bibliográficos
Main Authors: Rajcan‐Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
Assuntos:
Letter to JMG
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2598046/
https://ncbi.nlm.nih.gov/pubmed/16963482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.045013
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