MICROCEPHALY, MICROPHTHALMIA, FALCIFORM RETINAL FOLDS, AND BLINDNESS - A NEW SYNDROME

被引:26
作者
JARMAS, AL
WEAVER, DD
ELLIS, FD
DAVIS, A
机构
[1] INDIANA UNIV,SCH MED,DEPT MED GENET,INDIANAPOLIS,IN 46223
[2] INDIANA UNIV,SCH MED,DEPT OPHTHALMOL,INDIANAPOLIS,IN 46223
来源
AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1981年 / 135卷 / 10期
关键词
D O I
10.1001/archpedi.1981.02130340036013
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:930 / 933
页数:4
相关论文
共 24 条
[1]  
BLOMDAHL S, 1979, ACTA OPHTHALMOL, V57, P1048
[2]   AUTOSOMAL RECESSIVE MICROCEPHALY ASSOCIATED WITH CHORIORETINOPATHY [J].
CANTU, JM ;
ROJAS, JA ;
GARCIACRUZ, D ;
HERNANDEZ, A ;
PAGAN, P ;
FRAGOSO, R ;
MANZANO, C .
HUMAN GENETICS, 1977, 36 (02) :243-247
[3]   FAMILIAL NANOPHTHALMOS [J].
CROSS, HE ;
YODER, F .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1976, 81 (03) :300-306
[4]   Congenital retinal folds and microcephaly - Report of a case [J].
Gartner, S .
ARCHIVES OF OPHTHALMOLOGY, 1941, 25 (01) :93-100
[5]  
HAFEZ M, 1980, AM J HUM GENET, V32, pA109
[6]   AUTOSOMAL DOMINANT MICROCEPHALY [J].
HASLAM, RHA ;
SMITH, DW .
JOURNAL OF PEDIATRICS, 1979, 95 (05) :701-705
[7]  
HOEFNAGEL D, 1963, ARCH OPHTHALMOL-CHIC, V69, P760
[8]  
JANSSON F, 1963, ACTA OPHTHALMOL, V41, P25
[9]  
KLOEPFER H. WARNER, 1964, J GENET HUMAINE, V13, P52
[10]  
KOMAI T, 1955, AM J HUM GENET, V7, P51