Opitz GBBB syndrome and the 22q11.2 deletion

被引:0
作者
Lacassie, Y [1 ]
Arriaza, MI [1 ]
机构
[1] CHILDRENS HOSP,NEW ORLEANS,LA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 62卷 / 03期
关键词
D O I
10.1002/(SICI)1096-8628(19960329)62:3<318::AID-AJMG21>3.0.CO;2-M
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:318 / 318
页数:1
相关论文
共 3 条
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[2]   OPITZ-SYNDROME IS GENETICALLY HETEROGENEOUS, WITH ONE LOCUS ON XP22, AND A 2ND LOCUS ON 22Q11.2 [J].
ROBIN, NH ;
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[3]  
ZACKAI EH, 1995, 16 DW SMITH WORKSH M