THE SYNDROME OF RETINAL PIGMENTARY DEGENERATION, MICROCEPHALY, AND SEVERE MENTAL-RETARDATION (MIRHOSSEINI-HOLMES-WALTON SYNDROME) - REPORT OF 2 PATIENTS

被引:22
作者
MENDEZ, HMM [1 ]
PASKULIN, GA [1 ]
VALLANDRO, C [1 ]
机构
[1] FDN FAC FED CIENCIAS MED, NEUROL, BR-90000 PORTO ALEGRE, RS, BRAZIL
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1985年 / 22卷 / 02期
关键词
D O I
10.1002/ajmg.1320220202
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:223 / 228
页数:6
相关论文
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[2]   NEW FAMILIAL SYNDROME CHARACTERIZED BY PIGMENTARY RETINOPATHY, HYPOGONADISM, MENTAL-RETARDATION, NERVE DEAFNESS AND GLUCOSE-INTOLERANCE [J].
EDWARDS, JA ;
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