DOMINANT MIDFREQUENCY HEARING LOSS

被引：22
|
作者：
KONIGSMARK, BW
SALMAN, S
HASKINS, H
MENGEL, M
机构：
来源：
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY | 1970年 / 79卷 / 01期
关键词：
D O I：
10.1177/000348947007900105
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：42 / +
页数：1
相关论文
共 50 条
  • [21] Dominant hereditary conductive hearing loss due to an ossified stapedius tendon
    Hara, A
    Ase, Y
    Kusakari, J
    Kurosaki, Y
    ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 1997, 123 (10) : 1133 - 1135
  • [22] A dominant variant in DMXL2 is linked to nonsyndromic hearing loss
    Chen, Dong-Ye
    Liu, Xing-Feng
    Lin, Xiao-Jiang
    Zhang, Dan
    Chai, Yong-Chuan
    Yu, De-Hong
    Sun, Chang-Ling
    Wang, Xue-Ling
    Zhu, Wei-Dong
    Chen, Ying
    Sun, Lian-Hua
    Wang, Xiao-Wen
    Shi, Fu-Xin
    Huang, Zhi-Wu
    Yang, Tao
    Wu, Hao
    GENETICS IN MEDICINE, 2017, 19 (05) : 553 - 558
  • [23] Familial Autosomal Dominant Sensorineural Hearing Loss Associated with Dilated Cardiomyopathy
    Kaushik, Manu
    Alla, Venkata M.
    Madan, Ritu
    Reddy, Yeruva M.
    Nair, Chandra K.
    Gupta, Prateek K.
    SOUTHERN MEDICAL JOURNAL, 2010, 103 (12) : 1277 - 1278
  • [24] First implication of a hypophosphatemia gene in familial cases of dominant hearing loss
    Boussion, S.
    Vincent-Delorme, C.
    Briche, N.
    Broly, F.
    Manouvrier, S.
    Fajardy, I.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 186 - 187
  • [25] DETECTION OF NORMAL-HEARING CARRIERS OF THE GENE FOR THE AUTOSOMAL DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS
    STOLBOVA, D
    VALVODA, M
    ACTA OTO-LARYNGOLOGICA, 1985, 99 (5-6) : 509 - 515
  • [26] Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss
    Iwasaki, S
    Harada, D
    Usami, S
    Nagura, M
    Takeshita, T
    Hoshino, T
    ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2002, 128 (08) : 913 - 917
  • [27] Molecular analysis of an Australian family with late onset dominant hearing loss.
    Kamarinos, M
    Gardner, MJ
    Dahl, HHM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 312 - 312
  • [28] Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria
    Frohne, Alexandra
    Vrabel, Sybille
    Laccone, Franco
    Neesen, Juergen
    Roesch, Sebastian
    Dossena, Silvia
    Schoefer, Christian
    Frei, Klemens
    Parzefall, Thomas
    EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2024, 281 (07) : 3577 - 3586
  • [29] First independent confirmation of the PTPRQ gene involvement in autosomal dominant hearing loss
    Ozieblo, D.
    Adamiok, A.
    Sarosiak, A.
    Skarzynski, H.
    Oldak, M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 63 - 64
  • [30] The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss
    Yasukawa, Rika
    Moteki, Hideaki
    Nishio, Shin-ya
    Ishikawa, Kotaro
    Abe, Satoko
    Honkura, Yohei
    Hyogo, Misako
    Mihashi, Ryota
    Ikezono, Tetsuo
    Shintani, Tomoko
    Ogasawara, Noriko
    Shirai, Kyoko
    Yoshihashi, Hiroshi
    Ishino, Takashi
    Otsuki, Koshi
    Ito, Tsukasa
    Sugahara, Kazuma
    Usami, Shin-ichi
    GENES, 2019, 10 (10)
12345