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Interstitial Deletions at 6q14.1–q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype

BACKGROUND: Interstitial deletions of the long arm of chromosome 6 have been described in several patients with obesity and a Prader-Willi-like phenotype. Haploinsufficiency of the SIM1 gene located at 6q16.3 is suggested as being responsible for the regulation of body weight. Here we report on 2 pa...

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Detalhes bibliográficos
Main Authors: Wentzel, C., Lynch, S.A., Stattin, E.-L., Sharkey, F.H., Annerén, G., Thuresson, A.-C.
Formato: Artigo
Idioma:Inglês
Publicado em: S. Karger AG 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2941842/
https://ncbi.nlm.nih.gov/pubmed/21045960
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000314025
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