An unusual translocation within the Prader-Willi/Angelman syndrome critical region in 15q11-15q13 associated with clinical Prader-Willi syndrome.

被引：0
|
作者：
Schwartz, S
Grebe, T
Wolff, D
Becker, L
Conroy, J
Nicholls, RD
Horsthemke, B
Buiting, K
Cassidy, SB
机构：
[1] CASE WESTERN RESERVE UNIV,SCH MED,DEPT GENET,CLEVELAND,OH 44106
[2] CASE WESTERN RESERVE UNIV,SCH MED,CTR HUMAN GENET,CLEVELAND,OH
[3] UNIV HOSP CLEVELAND,CLEVELAND,OH
[4] UNIV ARIZONA,COLL MED,DEPT PEDIAT,TUCSON,AZ
[5] UNIV ESSEN GESAMTHSCH KLINIKUM,ESSEN,GERMANY
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 64卷 / 04期
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D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
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页码：3 / 3
页数：1
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