A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11-12 and on an atypical PWS patient with apparently normal karyotype.
作者信息
Kamei T, Hamabe J I, Matsumoto T, Abe K, Harada N, Ishikiriyama S, Hasegawa T, Miyazaki K, Mizuno S, Narahara K
出版信息
Jinrui Idengaku Zasshi. 1988 Dec;33(4):477-86. doi: 10.1007/BF01897789.
PMID:2907997
Abstract
摘要
Zotero 插件