Frequency of Births Due to Assisted Reproductive Technology (ART) in Prader-Willi Syndrome

PURPOSE: Prader-Willi syndrome (PWS) is an imprinting disorder characterized by typical facial, physical and cognitive/behavioral features, resulting from lack of paternally-expressed genes on chromosome 15q11.2-q13. Studies have suggested an increased risk of other imprinting disorders in children...

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Autors principals: Gold, June-Anne, Ruth, Chelsey, Osann, Kathryn, Flodman, Pamela, McManus, Barbara, Lee, Hye-Seung, Donkervoort, Sandra, Khare, Manaswitha, Roof, Elizabeth, Dykens, Elizabeth, Driscoll, Daniel J., Butler, Merlin G., Heinemann, Janalee, Cassidy, Suzanne, Kimonis, Virginia
Format: Artigo
Idioma:Inglês
Publicat: 2013
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4164429/
https://ncbi.nlm.nih.gov/pubmed/23928912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2013.97
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