Suggestive linkage of an autosomal dominant cataract locus (ADC 51) to chromosome 19q

被引：0
|
作者：
Turner, JL
Richter, L
Flodman, P
Chamberlain, W
von-Bischhoffshausen, FRB
Spence, MA
Bateman, JB
机构：
[1] Eleanor Roosevelt Inst, Denver, CO USA
[2] Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
[3] Univ Colorado, Rocky Mt Lions Eye Inst, Dept Ophthalmol, Denver, CO 80202 USA
[4] Univ Concepcion, Dept Oftalmol, Concepcion, Chile
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2003年 / 44卷
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
1261
引用
收藏
页码：U301 / U301
页数：1
相关论文
共 50 条
  • [31] A LOCUS FOR AUTOSOMAL DOMINANT SLEEPWALKING ON CHROMOSOME 20Q12-Q13.12
    Fisch, A.
    Desruisseau, D.
    Duntley, S.
    Gurnett, C. A.
    SLEEP, 2009, 32 : A293 - A293
  • [32] Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31
    Bisulli, Francesca
    Naldi, Ilaria
    Baldassari, Sara
    Magini, Pamela
    Licchetta, Laura
    Castegnaro, Giovanni
    Fabbri, Margherita
    Stipa, Carlotta
    Ferrari, Simona
    Seri, Marco
    Silva, Gilson Edmar Goncalves
    Tinuper, Paolo
    Pippucci, Tommaso
    EPILEPSIA, 2014, 55 (06) : 841 - 848
  • [33] Mapping of an autosomal recessive congenital cataract locus to chromosome 9q.
    Forshew, T
    Johnson, CA
    Maher, ER
    JOURNAL OF MEDICAL GENETICS, 2004, 41 : S82 - S82
  • [34] Mapping of an autosomal recessive congenital cataract locus to chromosome 9q.
    Forshew, T
    Johnson, CA
    Willis, C
    Moore, AT
    Maher, ER
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 489 - 489
  • [35] Mapping of an autosomal recessive congenital cataract locus to chromosome 9q.
    Forshew, T
    Johnson, CA
    Willis, C
    Moore, AT
    Maher, ER
    JOURNAL OF MEDICAL GENETICS, 2003, 40 : S86 - S86
  • [36] Autosomal dominant dilated cardiomyopathy: Clinical characterization and genetic linkage to a novel locus on chromosome 10q26
    Jha, S
    Mohiddin, SA
    Fananapazir, L
    Keating, MT
    CIRCULATION, 2002, 106 (19) : 61 - 61
  • [37] A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family
    Riazuddin, SA
    Yasmeen, A
    Zhang, QJ
    Yao, WL
    Sabar, MF
    Ahmed, Z
    Riazuddin, S
    Hejtmancik, JF
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46 (02) : 623 - 626
  • [38] A screen for mutations in the protein kinase C gamma gene in three families with autosomal dominant retinitis pigmentosa linked to the RP11 locus on chromosome 19q
    McEvoy, JA
    McGee, TL
    Berson, EL
    Dryja, TP
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1999, 40 (04) : S601 - S601
  • [39] Linkage analysis in an autosomal dominant ‘zonular nuclear pulverulent’ congenital cataract, mapped to chromosome 13q11-13
    Patrick Watts
    Mark Rees
    Angus Clarke
    Lyn Beck
    Carol Lane
    Michael J Owen
    Jonathon Gray
    Eye, 2000, 14 : 172 - 175
  • [40] Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13
    Watts, P
    Rees, M
    Clarke, A
    Beck, L
    Lane, C
    Owen, MJ
    Gray, J
    EYE, 2000, 14 (2) : 172 - 175
12345