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

被引：57

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：

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

页码：23 / 32

页数：10

共 27 条

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