NEW FAMILIAL SYNDROME CHARACTERIZED BY PIGMENTARY RETINOPATHY, HYPOGONADISM, MENTAL-RETARDATION, NERVE DEAFNESS AND GLUCOSE-INTOLERANCE

被引：58
作者：
EDWARDS, JA
SETHI, PK
SCOMA, AJ
BANNERMAN, RM
FROHMAN, LA
机构：
[1] BUFFALO GEN HOSP, DEPT MED, MED GENET UNIT, 100 HIGH ST, BUFFALO, NY 14203 USA
[2] BUFFALO GEN HOSP, DEPT NEUROL, BUFFALO, NY 14203 USA
[3] SUNY, DEPT MED, BUFFALO, NY USA
[4] SUNY, DEPT NEUROL, BUFFALO, NY USA
[5] EJ MEYER MEM HOSP, DEPT MED, BUFFALO, NY USA
[6] EJ MEYER MEM HOSP, DEPT NEUROL, BUFFALO, NY USA
来源：
AMERICAN JOURNAL OF MEDICINE | 1976年 / 60卷 / 01期
关键词：
D O I：
10.1016/0002-9343(76)90529-5
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：23 / 32
页数：10
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