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PARTIAL EXPRESSION OF ANGELMAN SYNDROME IN MOTHER MOST LIKELY TO BE DUE TO MOSAICISM INVOLVING BOTH SOMATIC AND GERMLINE CELLS

被引：2
作者：
HALL, JG
机构：
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 36卷 / 03期
关键词：
D O I：
10.1002/ajmg.1320360332
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：369 / 369
页数：1
相关论文
共 3 条
[1]  
HALL JG, 1988, AM J HUM GENET, V43, P355
[2]   ANGELMAN AND PRADER-WILLI SYNDROMES SHARE A COMMON CHROMOSOME-15 DELETION BUT DIFFER IN PARENTAL ORIGIN OF THE DELETION [J].
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NICHOLLS, RD ;
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LATT, SA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (02) :285-290
[3]   ANGELMAN SYNDROME IN A DAUGHTER WITH DEL(15) (Q11Q13) ASSOCIATED WITH BRACHYCEPHALY, HEARING-LOSS, ENLARGED FORAMEN MAGNUM, AND ATAXIA IN THE MOTHER [J].
WILLIAMS, CA ;
HENDRICKSON, JE ;
CANTU, ES ;
DONLON, TA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (03) :333-338
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