CHROMOSOME-13 LONG ARM INTERSTITIAL DELETION ASSOCIATED WITH FEATURES OF NOONAN PHENOTYPE

被引：0
作者：
ONUFER, CN
STEPHAN, MJ
THULINE, HC
CHAR, F
机构：
[1] MADIGAN ARMY MED CTR,DEPT PEDIAT,DISMORPHOL UNIT,TACOMA,WA 98431
[2] DEPT SOCIAL & HLTH SERV,DIV HLTH,CYTOGENET LAB,SEATTLE,WA 98155
[3] UNIV ARKANSAS MED SCI,PEDIAT,LITTLE ROCK,AR 72205
来源：
ANNALES DE GENETIQUE | 1987年 / 30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：236 / 239
页数：4
相关论文
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HUGHES, HE ;
PREUS, M ;
WITT, RD .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03) :507-514
[2]  
CHAR F, 1972, Birth Defects Original Article Series, V8, P110
[3]   NOONAN SYNDROME - A REVIEW [J].
MENDEZ, HMM ;
OPITZ, JM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03) :493-506
[4]  
NOEL B, 1976, CLIN GENET, V9, P593
[5]   HYPERTELORISM WITH TURNER PHENOTYPE - A NEW SYNDROME WITH ASSOCIATED CONGENITAL HEART DISEASE [J].
NOONAN, JA .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 116 (04) :373-&
[6]  
WILROY RS, 1983, AUG C MORPH MALF VAN, P19
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