PROBLEMS IN THE DETECTION OF 15Q DELETION IN PATIENTS WITH PRADER-WILLI SYNDROME

被引：0
|
作者：
WYANDT, HE
PATIL, S
SHAH, HO
HANSON, JW
ZELLWEGER, H
KELLY, TE
DOLAN, LM
WILSON, WG
机构：
[1] UNIV VIRGINIA,DEPT PEDIAT,CHARLOTTESVILLE,VA 22903
[2] UNIV IOWA,HOSP & CLIN,IOWA CITY,IA 52240
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1981年 / 33卷 / 06期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
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页码：A127 / A127
页数：1
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