EXCLUSION OF USHER SYNDROME GENE FROM MUCH OF CHROMOSOME-4

被引:39
作者
SMITH, RJH
HOLCOMB, JD
DAIGER, SP
CASKEY, CT
PELIAS, MZ
ALFORD, BR
FONTENOT, DD
HEJTMANCIK, JF
机构
[1] UNIV TEXAS,HLTH SCI CTR,HOUSTON,TX 77225
[2] LOUISIANA STATE UNIV,MED CTR,NEW ORLEANS,LA 70112
[3] LOUISIANA STATE DEPT EDUC,NEW ORLEANS,LA
来源
CYTOGENETICS AND CELL GENETICS | 1989年 / 50卷 / 2-3期
关键词
D O I
10.1159/000132733
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
收藏
页码:102 / 106
页数:5
相关论文
共 33 条
  • [1] BEATTY CW, 1979, MAYO CLIN PROC, V54, P543
  • [2] USHER SYNDROME - DEFINITION AND ESTIMATE OF PREVALENCE FROM 2 HIGH-RISK POPULATIONS
    BOUGHMAN, JA
    VERNON, M
    SHAVER, KA
    [J]. JOURNAL OF CHRONIC DISEASES, 1983, 36 (08): : 595 - 603
  • [3] BOUGHMAN JA, 1982, STRUCTURAL BIOCH ADV, P147
  • [4] Church G M, 1985, Prog Clin Biol Res, V177, P17
  • [5] DAIGER SP, 1987, CYTOGENET CELL GENET, V46, P602
  • [6] DAIGER SP, 1987, DEGENERATIVE RETINAL
  • [7] DAVENPORT SLH, 1977, INT C SERIES, V426, P87
  • [8] A GENETIC-LINKAGE MAP OF THE HUMAN GENOME
    DONISKELLER, H
    GREEN, P
    HELMS, C
    CARTINHOUR, S
    WEIFFENBACH, B
    STEPHENS, K
    KEITH, TP
    BOWDEN, DW
    SMITH, DR
    LANDER, ES
    BOTSTEIN, D
    AKOTS, G
    REDIKER, KS
    GRAVIUS, T
    BROWN, VA
    RISING, MB
    PARKER, C
    POWERS, JA
    WATT, DE
    KAUFFMAN, ER
    BRICKER, A
    PHIPPS, P
    MULLERKAHLE, H
    FULTON, TR
    NG, S
    SCHUMM, JW
    BRAMAN, JC
    KNOWLTON, RG
    BARKER, DF
    CROOKS, SM
    LINCOLN, SE
    DALY, MJ
    ABRAHAMSON, J
    [J]. CELL, 1987, 51 (02) : 319 - 337
  • [9] ISOLATION OF POLYMORPHIC DNA FRAGMENTS FROM HUMAN CHROMOSOME-4
    GILLIAM, TC
    HEALEY, ST
    MACDONALD, ME
    STEWART, GD
    WASMUTH, JJ
    TANZI, RE
    ROY, JC
    GUSELLA, JF
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (04) : 1445 - 1458
  • [10] THE POSITIONS OF 3 RESTRICTION FRAGMENT LENGTH POLYMORPHISMS ON CHROMOSOME-4 RELATIVE TO KNOWN GENETIC-MARKERS
    GILLIAM, TC
    SCAMBLER, P
    ROBBINS, T
    INGLE, C
    WILLIAMSON, R
    DAVIES, KE
    [J]. HUMAN GENETICS, 1984, 68 (02) : 154 - 158