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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados