FAMILIAL CONGENITAL MONOCHROMATISM, CATARACTS, AND SENSORINEURAL DEAFNESS

被引：3

作者：

JAN, JE

TZE, WJ

JOHNSTON, AC

DUNN, HG

机构：

[1] UNIV BRITISH COLUMBIA,DEPT PEDIAT,VANCOUVER V6T 1W5,BRITISH COLUMBI,CANADA

[2] UNIV BRITISH COLUMBIA,DEPT OPHTHALMOL,VANCOUVER V6T 1W5,BRITISH COLUMBI,CANADA

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1976年 / 130卷 / 12期

关键词：

D O I：

10.1001/archpedi.1976.02120130055011

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：1349 / 1350

页数：2

共 6 条

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ALPERN, M
FALLS, HF
LEE, GB
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[2] Andersen S. Ry, 1946, ADA OPHTHALMOL [COPENHAGEN], V24, P99
[3] TYPICAL TOTAL MONOCHROMACY - A HISTOLOGICAL AND PSYCHOPHYSICAL STUDY
FALLS, HF
WOLTER, JR
ALPERN, M
[J]. ARCHIVES OF OPHTHALMOLOGY, 1965, 74 (05) : 610 - &
[4] FRANCOIS J, 1959, ARCH OPHTALMOL-PARIS, V19, P245
[5] SIGNIFICANCE OF INTERMEDIATE PLASMA GROWTH-HORMONE LEVELS IN GROWTH-RETARDED CHILDREN
JOSS, EE
ZUPPINGER, KA
[J]. JOURNAL OF PEDIATRICS, 1972, 81 (06) : 1092 - +
[6] MADSEN PH, 1967, ACTA OPHTHALMOL, V45, P587