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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 no: | Genet Med |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | 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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