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

[11]

FUNDERBURK SJ, 1974, AM J HUM GENET, V26, P715

[12] Bilateral acoustic neurofibromas - A clinical study and field survey of a family of five generations with bilateral deafness in thirty-eight members [J].

Gardner, WJ ;

Frazier, CH .

ARCHIVES OF NEUROLOGY AND PSYCHIATRY, 1930, 23 (02) :266-302

[13]

GOLDBERG MF, 1986, ARCH OPHTHALMOL-CHIC, V76, P797

[14]

GORDON AM, 1976, JOHNS HOPKINS MED J, V138, P142

[15]

GRONDAHL J, 1987, CLIN GENET, V31, P255

[16]

HAGEMAN MJ, 1977, AM J HUM GENET, V29, P468

[17]

HAMMERSCHLAG V, 1907, Z OHRENHEILKD, V54, P18

[18] TENTATIVE ASSIGNMENT OF PIEBALD TRAIT GENE TO CHROMOSOME BAND 4Q12 [J].

HOO, JJ ;

HASLAM, RHA ;

VANORMAN, C .

HUMAN GENETICS, 1986, 73 (03) :230-231

[19] WAARDENBURG SYNDROME TYPE-I IN A CHILD WITH DENOVO INVERSION (2)(Q35Q37.3) [J].

ISHIKIRIYAMA, S ;

TONOKI, H ;

SHIBUYA, Y ;

CHIN, S ;

HARADA, N ;

ABE, K ;

NIIKAWA, N .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 33 (04) :505-507

[20]

JAY M, 1982, BIRTH DEFECTS-ORIG, V18, P167

← 1 2 3 4 5 6 →