Gene localization for aculeiform cataract, on chromosome 2q33-35

被引：20
|
作者：
Héon, E
Liu, S
Billingsley, G
Bernasconi, O
Tsifildis, C
Schorderet, DF
Munier, FL
机构：
[1] Eye Res Inst Canada, Toronto, ON M5T 2S8, Canada
[2] Univ Toronto, Dept Ophthalmol, Toronto, ON, Canada
[3] Div Med Genet, Mol Genet Unit, Lausanne, Switzerland
[4] Hop Ophtalm Jules Gonin, Lausanne, Switzerland
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 63卷 / 03期
关键词：
D O I：
10.1086/302005
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：921 / 926
页数：6
相关论文
共 50 条
  • [1] Gene localization for aculeiform cataract, on chromosome 2q33-35 (vol 63, pg 921, 1998)
    Heon
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (01) : 334 - 334
  • [2] Mapping of congenital aculeiform cataract to chromosome 2q33
    Heon, E
    Munier, F
    Tsifildis, C
    Liu, S
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1997, 38 (04) : 4348 - 4348
  • [3] Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35
    Rogaev, EI
    Rogaeva, EA
    Korovaitseva, GI
    Farrer, LA
    Petrin, AN
    Keryanov, SA
    Turaeva, S
    Chumakov, I
    StGeorgeHyslop, P
    Ginter, EK
    HUMAN MOLECULAR GENETICS, 1996, 5 (05) : 699 - 703
  • [4] Mapping of a second locus for Lamellar ichthyosis to chromosome 2q33-35
    Parmentier, L
    Lakhdar, H
    BlanchetBardon, C
    Marchand, S
    Dubertret, L
    Weissenbach, J
    HUMAN MOLECULAR GENETICS, 1996, 5 (04) : 555 - 559
  • [5] Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35 (vol 5, pg 555, 1996)
    Parmentier, L
    Lakhdar, H
    BlanchetBardon, C
    Marchand, S
    Dubertret, L
    Weissenbach, J
    HUMAN MOLECULAR GENETICS, 1996, 5 (06) : 862 - 863
  • [6] Mutation of gamma crastallin gene on chromosome 2q33-q35 and the autosomal dominant zonular pulverulent cataract.
    Ren, ZX
    Li, A
    Shastry, BS
    Padma, T
    Ayyagari, R
    Scott, MH
    Parks, MM
    Kaiser-Kupfer, MI
    Hejtmancik, JF
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S97 - S97
  • [7] Infantile onset progressive ascending spastic paralysis is linkes to ALS2/Alsin gene on 2q33-35
    Eymard-Pierre, E
    Bertini, E
    Lesca, G
    di Capua, M
    Cusmai, R
    Leuzzi, V
    Ponsone, A
    Boespflug-Tanguy, O
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 273 - 273
  • [8] LOCALIZATION OF THE VILLIN GENE ON HUMAN-CHROMOSOME 2Q35-Q36 AND ON MOUSE CHROMOSOME-1
    ROUSSEAUMERCK, MF
    SIMONCHAZOTTES, D
    ARPIN, M
    PRINGAULT, E
    LOUVARD, D
    GUENET, JL
    BERGER, R
    HUMAN GENETICS, 1988, 78 (02) : 130 - 133
  • [9] LOCALIZATION OF THE HUMAN GAMMA-CRYSTALLIN GENE-CLUSTER (CRYG) TO THE LONG ARM OF CHROMOSOME-2, REGION Q33-Q35
    TSUI, LC
    BREITMAN, ML
    MEAKIN, SO
    WILLARD, HF
    SHILOH, Y
    DONLON, T
    BRUNS, G
    CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 763 - 764
  • [10] LOCALIZATION OF THE VILLIN STRUCTURAL GENE TO HUMAN-CHROMOSOME 2Q35-Q36 AND TO MOUSE CHROMOSOME-1
    ROUSSEAUMERCK, MF
    SIMONCHAZOTTES, D
    ARPIN, M
    PRINGAULT, E
    LOUVARD, D
    GUENET, JL
    BERGER, R
    CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4): : 685 - 685
12345