AUTOSOMAL RECESSIVE PROGRESSIVE HIGH-FREQUENCY SENSORINEURAL DEAFNESS IN CHILDHOOD

被引：0
|
作者：
CREMERS, CWRJ
VANRIJN, P
TERHAAR, BGA
机构：
来源：
CLINICAL OTOLARYNGOLOGY | 1987年 / 12卷 / 02期
关键词：
D O I：
暂无
中图分类号：
R76 [耳鼻咽喉科学];
学科分类号：
100213 ;
摘要：
引用
收藏
页码：145 / 145
页数：1
相关论文
共 50 条
  • [1] AUTOSOMAL RECESSIVE PROGRESSIVE HIGH-FREQUENCY SENSORINEURAL DEAFNESS IN CHILDHOOD
    CREMERS, C
    VANRIJN, P
    TERHAAR, B
    [J]. ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 1987, 113 (12) : 1319 - 1324
  • [2] AUTOSOMAL RECESSIVE NON-SYNDROMAL PROGRESSIVE SENSORINEURAL DEAFNESS IN CHILDHOOD - SEPARATE CLINICAL AND GENETIC ENTITY
    CREMERS, CWRJ
    [J]. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1979, 1 (03) : 193 - 199
  • [3] FAMILIAL AUTOSOMAL RECESSIVE HYDROCEPHALUS WITH SENSORINEURAL DEAFNESS
    RONEN, GM
    FRASER, FC
    HENEGHAN, WD
    HOBEIKA, C
    JACOB, JC
    MAROUN, FB
    [J]. CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1986, 13 (02) : 193 - 193
  • [4] HETEROGENEITY OF DOMINANT HIGH-FREQUENCY SENSORINEURAL DEAFNESS
    HIGASHI, K
    [J]. CLINICAL GENETICS, 1988, 33 (06) : 424 - 428
  • [5] AUTOSOMAL RECESSIVE SENSORINEURAL DEAFNESS AND CONGENITAL ABSENCE OF THE THYROID
    TOOMEY, KE
    MOYER, SL
    REZVANI, I
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 152 - 152
  • [6] AUTOSOMAL RECESSIVE SENSORINEURAL DEAFNESS - COMPARISON OF 2 KINDREDS
    MCLEOD, AC
    SWEENEY, A
    MCCONNELL, FE
    KEMKER, FJ
    NANCE, WE
    WEBB, WW
    [J]. SOUTHERN MEDICAL JOURNAL, 1973, 66 (01) : 141 - 152
  • [7] RENAL TUBULAR-ACIDOSIS AND SENSORINEURAL DEAFNESS - AN AUTOSOMAL RECESSIVE SYNDROME
    CREMERS, CWRJ
    MONNENS, LAH
    MARRES, EHMA
    [J]. ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 1980, 106 (05) : 287 - 289
  • [8] A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness
    Frei, K
    Lucas, T
    Ramsebner, R
    Schöfer, C
    Baumgartner, WD
    Weipoltshammer, K
    Erginel-Unaltuna, N
    Wachtler, FJ
    Kirschhofer, K
    [J]. AUDIOLOGY AND NEURO-OTOLOGY, 2004, 9 (01) : 47 - 50
  • [9] AUTOSOMAL RECESSIVE UNCOMPLICATED PROFOUND CHILDHOOD DEAFNESS IN AN ARABIC FAMILY WITH HIGH CONSANGUINITY
    KABARITY, A
    ALAWADI, SA
    FARAG, TI
    MALLALAH, G
    [J]. HUMAN GENETICS, 1981, 57 (04) : 444 - 446
  • [10] A NEW FORM OF X-LINKED, HIGH-FREQUENCY, SENSORINEURAL DEAFNESS
    WELLESLEY, D
    GOLDBLATT, J
    [J]. CLINICAL GENETICS, 1992, 41 (02) : 79 - 81
12345