Obesity in adults with 22q11.2 deletion syndrome

PURPOSE: To characterize the prevalence of and contributing factors to adult obesity in the most common recurrent copy number variation (CNV), 22q11.2 deletion, given that other rare CNVs are known to have obesity phenotypes. METHODS: For 207 adults with 22q11.2 deletion syndrome (22q11.2DS), we use...

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Publicado en:Genet Med
Main Authors: Voll, S, Boot, E, Butcher, N, Cooper, S, Heung, T, Chow, EWC, Silversides, C, Bassett, AS
Formato: Artigo
Idioma:Inglês
Publicado: 2016
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5292049/
https://ncbi.nlm.nih.gov/pubmed/27537705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2016.98
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