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

[31]

OSWALD AH, 1985, S AFR MED J, V68, P863

[32] LINKAGE STUDIES OF USHER SYNDROME - ANALYSIS OF AN ACADIAN KINDRED IN LOUISIANA [J].

PELIAS, MZ ;

LEMOINE, DR ;

KOSSAR, AL ;

WARD, LJ ;

WILSON, AF ;

ELSTON, RC .

CYTOGENETICS AND CELL GENETICS, 1988, 47 (1-2) :111-112

[33] GENETIC-LINKAGE OF BILATERAL ACOUSTIC NEUROFIBROMATOSIS TO A DNA MARKER ON CHROMOSOME-22 [J].

ROULEAU, GA ;

WERTELECKI, W ;

HAINES, JL ;

HOBBS, WJ ;

TROFATTER, JA ;

SEIZINGER, BR ;

MARTUZA, RL ;

SUPERNEAU, DW ;

CONNEALLY, PM ;

GUSELLA, JF .

NATURE, 1987, 329 (6136) :246-248

[34]

ROZYCKI DL, 1971, ARCHIV OTOLARYNGOL, V93, P194

[35] UNIVERSAL DYSCHROMATOSIS, SMALL STATURE AND HIGH-TONE DEAFNESS [J].

RYCROFT, RJG ;

CALNAN, CD ;

WELLS, RS .

CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1977, 2 (01) :45-48

[36] LOSS OF GENES ON CHROMOSOME-22 IN TUMORIGENESIS OF HUMAN ACOUSTIC NEUROMA [J].

SEIZINGER, BR ;

MARTUZA, RL ;

GUSELLA, JF .

NATURE, 1986, 322 (6080) :644-647

[37]

SELLARS S, 1977, S AFR MED J, V51, P309

[38] CHILDHOOD DEAFNESS IN SOUTHERN-AFRICA - AN ETIOLOGICAL SURVEY OF 3,064 DEAF-CHILDREN [J].

SELLARS, S ;

BEIGHTON, P .

JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1983, 97 (10) :885-889

[39]

SELLARS S, 1975, S AFR MED J, V49, P1135

[40]

SELLARS S, 1976, S AFR MED J, V50, P1193

← 1 2 3 4 5 6 →