Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15 - A coincidence?

被引：0
|
作者：
Butler, MG
Hedges, LK
Rogan, PK
Seip, JR
Cassidy, SB
Moeschler, JB
机构：
[1] VANDERBILT UNIV,DEPT PATHOL,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,DEPT ORTHOPED,NASHVILLE,TN 37232
[3] PENN STATE UNIV,MILTON S HERSHEY MED CTR,DEPT PEDIAT,HERSHEY,PA 17033
[4] CASE WESTERN RESERVE UNIV,DEPT GENET,CLEVELAND,OH 44106
[5] UNIV HOSP CLEVELAND,CTR HUMAN GENET,CLEVELAND,OH 44106
[6] DARTMOUTH HITCHCOCK MED CTR,CTR GENET & CHILD DEV,LEBANON,NH 03766
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 72卷 / 01期
关键词：
D O I：
10.1002/(SICI)1096-8628(19971003)72:1<111::AID-AJMG22>3.0.CO;2-T
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：111 / 114
页数：4
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