MOLECULAR-GENETICS OF X-LINKED HEARING IMPAIRMENT

被引:9
作者
BRUNNER, HG [1 ]
SMEETS, B [1 ]
SMEETS, D [1 ]
NELEN, M [1 ]
CREMERS, CWRJ [1 ]
ROPERS, HH [1 ]
机构
[1] UNIV HOSP NIJMEGEN, DEPT OTORHINOLARYNGOL, 6500 HB NIJMEGEN, NETHERLANDS
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.tb19586.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
收藏
页码:176 / 190
页数:15
相关论文
共 54 条
  • [1] RE-EVALUATION OF NEW X-LINKED SYNDROME FOR EVIDENCE OF CHARGE SYNDROME OR ASSOCIATION
    ABRUZZO, MA
    ERICKSON, RP
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (03): : 397 - 400
  • [2] ATKIN CL, 1988, AM J HUM GENET, V42, P249
  • [3] CONTIGUOUS GENE SYNDROMES DUE TO DELETIONS IN THE DISTAL SHORT ARM OF THE HUMAN X-CHROMOSOME
    BALLABIO, A
    BARDONI, B
    CARROZZO, R
    ANDRIA, G
    BICK, D
    CAMPBELL, L
    HAMEL, B
    FERGUSONSMITH, MA
    GIMELLI, G
    FRACCARO, M
    MARASCHIO, P
    ZUFFARDI, O
    GUIOLI, S
    CAMERINO, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) : 10001 - 10005
  • [4] IDENTIFICATION OF MUTATIONS IN THE COL4A5 COLLAGEN GENE IN ALPORT SYNDROME
    BARKER, DF
    HOSTIKKA, SL
    ZHOU, J
    CHOW, LT
    OLIPHANT, AR
    GERKEN, SC
    GREGORY, MC
    SKOLNICK, MH
    ATKIN, CL
    TRYGGVASON, K
    [J]. SCIENCE, 1990, 248 (4960) : 1224 - 1227
  • [5] FABRY DISEASE - 6 GENE REARRANGEMENTS AND AN EXONIC POINT MUTATION IN THE ALPHA-GALACTOSIDASE GENE
    BERNSTEIN, HS
    BISHOP, DF
    ASTRIN, KH
    KORNREICH, R
    ENG, CM
    SAKURABA, H
    DESNICK, RJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (04) : 1390 - 1399
  • [6] CLOSE LINKAGE BETWEEN NORRIE DISEASE, A CLONED DNA-SEQUENCE FROM THE PROXIMAL SHORT ARM, AND THE CENTROMERE OF THE X-CHROMOSOME
    BLEEKERWAGEMAKERS, LM
    FRIEDRICH, U
    GAL, A
    WIENKER, TF
    WARBURG, M
    ROPERS, HH
    [J]. HUMAN GENETICS, 1985, 71 (03) : 211 - 214
  • [7] AUDIOMETRIC EVIDENCE FOR 2 FORMS OF X-LINKED HYPOPHOSPHATEMIA IN HUMANS, APPARENT COUNTERPARTS OF HYP AND GY MUTATIONS IN MOUSE
    BONEH, A
    READE, TM
    SCRIVER, CR
    RISHIKOF, E
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 27 (04): : 997 - 1003
  • [8] THE GENE FOR X-LINKED PROGRESSIVE MIXED DEAFNESS WITH PERILYMPHATIC GUSHER DURING STAPES SURGERY (DFN3) IS LINKED TO PGK
    BRUNNER, HG
    VANBENNEKOM, CA
    LAMBERMON, EMM
    OEI, TL
    CREMERS, CWRJ
    WIERINGA, B
    ROPERS, HH
    [J]. HUMAN GENETICS, 1988, 80 (04) : 337 - 340
  • [9] BRUNNER HG, KIDNEY INT, V34, P7
  • [10] X-LINKED MOTOR-SENSORY NEUROPATHY TYPE-II WITH DEAFNESS AND MENTAL-RETARDATION - A NEW DISORDER
    COWCHOCK, FS
    DUCKETT, SW
    STRELETZ, LJ
    GRAZIANI, LJ
    JACKSON, LG
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 20 (02): : 307 - 315