A new locus for dominant progressive hearing loss DFNA37 mapped to chromosome 1p21.

被引:0
|
作者
Talebizadeh, Z
Kenyon, JB
Askew, JW
Smith, SD
机构
[1] Boys Town Natl Res Hosp, Omaha, NE 68131 USA
[2] Univ Nebraska, Med Ctr, Omaha, NE USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
1740
引用
收藏
页码:314 / 314
页数:1
相关论文
共 50 条
  • [31] A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25
    Morell, RJ
    Friderici, KH
    Wei, SN
    Elfenbein, JL
    Friedman, TB
    Fisher, RA
    GENOMICS, 2000, 63 (01) : 1 - 6
  • [32] Linkage analysis of progressive hearing loss in five extended families maps the DFNA1 gene to a 1.25-Mb region on chromosome 1p
    VanCamp, G
    Coucke, PJ
    Kunst, H
    Schatteman, I
    VanVelzen, D
    Marres, H
    vanEwijk, M
    Declau, F
    VanHauwe, P
    Meyers, J
    Kenyon, J
    Smith, SD
    Smith, RJH
    Djelantik, B
    Cremers, CWRJ
    VandeHeyning, PH
    Willems, PJ
    GENOMICS, 1997, 41 (01) : 70 - 74
  • [33] Mapping of a new autosomal dominant non-syndromic hearing loss (DFNA43) to chromosome 2q12.
    Flex, E
    Mangino, M
    Mazzoli, M
    Martini, A
    Pizzuti, A
    Dallapiccola, B
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 452 - 452
  • [34] A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15
    Boensch, D.
    Schmidt, C. M.
    Scheer, P.
    Bohlender, J.
    Neumann, C.
    Zehnhoff-Dinnesen, A. am
    Deufel, T.
    HNO, 2008, 56 (02) : 177 - 182
  • [35] A new gene for autosomal dominant nonsyndromic sensorineural hearing loss (DFNA32) maps to 11p15.
    Li, XC
    Saal, HM
    Friedman, TB
    Friedman, RA
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 312 - 312
  • [36] A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter
    Boensch, D.
    Schmidt, C. -M.
    Scheer, P.
    Bohlender, J.
    Neumann, C.
    Zehnhoff-Dinnesen, A. Am
    Deufel, T.
    HNO, 2009, 57 (04) : 371 - 376
  • [37] DFNA53: A new locus for autosomal dominant hearing loss maps to 14q11.2-22.1 in a large family from China.
    Pandya, A
    Blanton, SH
    Yan, D
    Ke, X
    Ouyang, XM
    Du, LL
    Balkany, T
    Nance, WE
    Liu, XZ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 466 - 466
  • [38] Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p-13.3-22.1.
    Masmoudi, S
    Tlili, A
    Ghorbel, A
    Chardenoux, S
    Lemainque, A
    Majava, M
    Ben Zina, Z
    Mala, J
    Mannikko, M
    Weil, D
    Lathrop, M
    Ala-Kokko, L
    Drira, M
    Petit, C
    Ayadi, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 511 - 511
  • [39] Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1
    Saber Masmoudi
    Abdelaziz Tlili
    Marja Majava
    Abdel Monem Ghorbel
    Sébastien Chardenoux
    Arnaud Lemainque
    Zeineb Ben Zina
    Jihene Moala
    Minna Männikkö
    Dominique Weil
    Mark Lathrop
    Leena Ala-Kokko
    Mohamed Drira
    Christine Petit
    Hammadi Ayadi
    European Journal of Human Genetics, 2003, 11 : 185 - 188
  • [40] Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1
    Masmoudi, S
    Tlili, A
    Majava, M
    Ghorbel, AM
    Chardenoux, S
    Lemainque, A
    Ben Zina, Z
    Moala, J
    Männikkö, M
    Weil, D
    Lathrop, M
    Ala-Kokko, L
    Drira, M
    Petit, C
    Ayadi, H
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2003, 11 (02) : 185 - 188