WAARDENBURG-LIKE FEATURES WITH CATARACTS, SMALL HEAD SIZE, JOINT ABNORMALITIES, HYPOGONADISM, AND OSTEOSARCOMA

被引:8
作者
PARRY, DM
SAFYER, AW
MULVIHILL, JJ
机构
关键词
D O I
10.1136/jmg.15.1.66
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:66 / 69
页数:4
相关论文
共 11 条
[1]  
ARIAS S, 1971, Birth Defects Original Article Series, V7, P87
[2]   MAJOR HISTOCOMPATIBILITY COMPLEX - GENETICS AND BIOLOGY .1. [J].
BACH, FH ;
VANROOD, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (15) :806-813
[3]   NEW FAMILIAL SYNDROME CHARACTERIZED BY PIGMENTARY RETINOPATHY, HYPOGONADISM, MENTAL-RETARDATION, NERVE DEAFNESS AND GLUCOSE-INTOLERANCE [J].
EDWARDS, JA ;
SETHI, PK ;
SCOMA, AJ ;
BANNERMAN, RM ;
FROHMAN, LA .
AMERICAN JOURNAL OF MEDICINE, 1976, 60 (01) :23-32
[4]   WERNERS SYNDROME - A REVIEW OF ITS SYMPTOMATOLOGY NATURAL HISTORY PATHOLOGIC FEATURES GENETICS AND RELATIONSHIP TO NATURAL AGING PROCESS [J].
EPSTEIN, CJ ;
MARTIN, GM ;
SCHULTZ, AL ;
MOTULSKY, AG .
MEDICINE, 1966, 45 (03) :177-+
[5]  
FRASER GR, 1976, CAUSES PROFOUND DEAF, P90
[6]  
FRAUMENI JF, 1975, PRIMARY BONE CANCER, P17
[7]  
GOLDBERG NH, CANCER
[8]  
RIMOIN DL, 1971, GENETIC DISORDERS EN, P305
[9]  
Sieber S M, 1975, Adv Cancer Res, V22, P57
[10]  
SOUSSI JT, 1974, LIGHT EYED NEGROES K, P14