HEARING IMPAIRMENT AND PIGMENTARY DISTURBANCE

被引：10

作者：

BEIGHTON, P

RAMESAR, R

WINSHIP, I

VILJOEN, D

GREENBERG, J

YOUNG, K

CURTIS, D

SELLARS, S

机构：

[1] UNIV CAPE TOWN, SCH MED, DEPT OTOLARYNGOL, CAPE TOWN 7925, SOUTH AFRICA

[2] UNIV SHEFFIELD, DEPT MED GENET, SHEFFIELD S10 2TN, S YORKSHIRE, ENGLAND

来源：

ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES | 1991年 / 630卷

关键词：

D O I：

10.1111/j.1749-6632.1991.tb19584.x

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

[No abstract available]

引用

页码：152 / 166

页数：15

共 54 条

[1]

ARIAS S, 1975, HUMANGENETIK, V27, P145

[2]

ARIAS S, 1971, Birth Defects Original Article Series, V7, P87

[3]

BEIGHTON P, 1987, S AFR MED J, V72, P209

[4] USHER SYNDROME - DEFINITION AND ESTIMATE OF PREVALENCE FROM 2 HIGH-RISK POPULATIONS [J].

BOUGHMAN, JA ;

VERNON, M ;

SHAVER, KA .

JOURNAL OF CHRONIC DISEASES, 1983, 36 (08) :595-603

[5]

DAIGER SP, 1987, CYTOGENET CELL GENET, V46, P602

[6] USHERS SYNDROME - WITH SPECIAL REFERENCE TO HETEROZYGOUS MANIFESTATIONS [J].

DEHAAS, EBH ;

VANLITH, GHM ;

RIJNDERS, J ;

RUMKE, AML ;

VOLMER, C .

DOCUMENTA OPHTHALMOLOGICA, 1970, 28 (01) :166-&

[7]

DELLEMAN JW, 1978, J PEDIAT OPHTH STRAB, V15, P341

[8] NEW FAMILIAL SYNDROME CHARACTERIZED BY PIGMENTARY RETINOPATHY, HYPOGONADISM, MENTAL-RETARDATION, NERVE DEAFNESS AND GLUCOSE-INTOLERANCE [J].

EDWARDS, JA ;

SETHI, PK ;

SCOMA, AJ ;

BANNERMAN, RM ;

FROHMAN, LA .

AMERICAN JOURNAL OF MEDICINE, 1976, 60 (01) :23-32

[9]

FOY C, 1990, AM J HUM GENET, V46, P1017

[10]

FRASER G R, 1964, J Med Genet, V1, P118, DOI 10.1136/jmg.1.2.118

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