Prenatal genetic testing for a microdeletion at chromosome 14q32.2 imprinted region leading to UPD(14)pat-like phenotype.
作者信息
Sasaki Aiko, Sumie Masahiro, Wada Seiji, Kosaki Rika, Kurosawa Kenji, Fukami Maki, Sago Haruhiko, Ogata Tsutomu, Kagami Masayo
机构信息
Department of Maternal-Fetal and Neonatal Medicine, National Center for Child Health and Development, Tokyo, Japan.
出版信息
Am J Med Genet A. 2014 Jan;164A(1):264-6. doi: 10.1002/ajmg.a.36185. Epub 2013 Nov 20.
PMID:24259232
Abstract
摘要
Zotero 插件