SYNDROME OF MENTAL-RETARDATION, SEIZURES, HYPOTONIC CEREBRAL-PALSY AND MEGALOCORNEAE, RECESSIVELY INHERITED

被引:33
作者
NEUHAUSER, G
KAVEGGIA, EG
FRANCE, TD
OPTIZ, JM
机构
[1] UNIV WISCONSIN,HARRY A WAISMAN CTR MENTAL RETARDATION & HUMAN DEV,MADISON,WI
[2] CENT WISCONSIN COLONY & TRAINING SCH,MADISON,WI
[3] UNIV WISCONSIN,CTR HLTH SCI & MED SCH,DEPT PEDIAT,MADISON,WI
[4] WISCONSIN CLIN GENET CTR,DEPT PEDIAT,MADISON,WI
[5] WISCONSIN CLIN GENET CTR,DEPT MED GENET,MADISON,WI
[6] UNIV WISCONSIN,CTR HLTH SCI & MED SCH,DEPT PEDIAT,109 GENET BLDG,MADISON,WI 53706
来源
ZEITSCHRIFT FUR KINDERHEILKUNDE | 1975年 / 120卷 / 01期
关键词
D O I
10.1007/BF00443795
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:1 / 18
页数:18
相关论文
共 23 条
[1]  
AITA JA, 1969, CONGENITAL FACIAL AN
[2]  
[Anonymous], 1961, HEREDITY OPHTHALMOLO
[3]  
CALAMANDREI G, 1950, G ITAL OFTAL, V3, P278
[4]  
COLLIER M, 1971, ACTA OPHTHALMOL, V49, P946
[5]  
COLLINS ET, 1920, T OPHTHAL SOC UK, V40, P132
[6]  
Dessoff J, 1934, ARCH OPHTHALMOL-CHIC, V12, P60
[7]  
DUKEELDER S, 1963, SYSTEM OPHTHALMOLO 2, V3
[8]  
FOERSTER O, 1910, DTSCH ARCH KLIN MED, V98, P216
[9]  
FRANCESCHETTI A, 1961, GENETICS OPHTHALMOLO, V1
[10]  
FRANK Y, 1973, J GENET HUM, V21, P67