NOONAN PHENOTYPE ASSOCIATED WITH NEUROFIBROMATOSIS

被引:89
作者
ALLANSON, JE
HALL, JG
VANALLEN, MI
机构
[1] UNIV BRITISH COLUMBIA,CLIN GENET UNIT,4490 OAK ST,VANCOUVER V6H 3V5,BC,CANADA
[2] SW BIOMED RES INST,CTR GENET,TEMPE,AZ 85281
[3] UNIV WASHINGTON,SEATTLE,WA 98195
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1985年 / 21卷 / 03期
关键词
D O I
10.1002/ajmg.1320210307
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:457 / 462
页数:6
相关论文
共 8 条
[1]   FAMILIAL ASSOCIATION OF NEUROFIBROMATOSIS, PERONEAL MUSCULAR-ATROPHY, CONGENITAL DEAFNESS, PARTIAL ALBINISM, AND AXENFELDS DEFECT [J].
BRADLEY, WG ;
RICHARDSON, J ;
FREW, IJC .
BRAIN, 1974, 97 (SEP) :521-+
[2]  
CROWE SW, 1956, CLIN PATHOLOGICAL GE
[3]   COINCIDENCE OF NEUROFIBROMATOSIS AND MYOTONIC-DYSTROPHY IN A KINDRED [J].
ICHIKAWA, K ;
CROSLEY, CJ ;
CULEBRAS, A ;
WEITKAMP, L .
JOURNAL OF MEDICAL GENETICS, 1981, 18 (02) :134-138
[4]  
MENDEZ HMM, 1983, NEUROFIBROMATOSIS NO, V3, P158
[5]  
MONTEL M, 1925, ARCH MED PHARM MILIT, V83, P77
[6]   VONRECKLINGHAUSEN NEUROFIBROMATOSIS [J].
RICCARDI, VM .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (27) :1617-1627
[7]  
ROSENBLATT B, 1983, AM J HUM GENET
[8]  
SMITH DW, 1981, RECOGNIZABLE PATTERN, P130