SPECIFIC READING-DISABILITY - IDENTIFICATION OF AN INHERITED FORM THROUGH LINKAGE ANALYSIS

被引:256
作者
SMITH, SD
KIMBERLING, WJ
PENNINGTON, BF
机构
[1] UNIV COLORADO,CTR HLTH SCI,DEPT PSYCHIAT,DENVER,CO 80262
[2] UNIV MIAMI,MAILMAN CTR CHILD DEV,MIAMI,FL 33101
关键词
D O I
10.1126/science.6828864
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
引用
收藏
页码:1345 / 1347
页数:3
相关论文
共 12 条
  • [1] A NEUROLOGICAL APPRAISAL OF FAMILIAL CONGENITAL WORD-BLINDNESS
    DREW, AL
    [J]. BRAIN, 1956, 79 (03) : 440 - 460
  • [2] GENETICS OF SPECIFIC READING-DISABILITY
    FINUCCI, JM
    GUTHRIE, JT
    CHILDS, AL
    ABBEY, H
    CHILDS, B
    [J]. ANNALS OF HUMAN GENETICS, 1976, 40 (JUL) : 1 - 23
  • [3] HALLGREN B, 1950, ACTA PSYCHIATRIC N S, V65
  • [4] GENETIC MODELS OF READING-DISABILITY
    LEWITTER, FI
    DEFRIES, JC
    ELSTON, RC
    [J]. BEHAVIOR GENETICS, 1980, 10 (01) : 9 - 30
  • [5] Lubs H A, 1973, Methods Cell Biol, V6, P345, DOI 10.1016/S0091-679X(08)60057-6
  • [6] HUMAN Q AND C CHROMOSOMAL VARIATIONS - DISTRIBUTION AND INCIDENCE
    MCKENZIE, WH
    LUBS, HA
    [J]. CYTOGENETICS AND CELL GENETICS, 1975, 14 (02): : 97 - 115
  • [7] MILLER OJ, 1975, JUL WORKSH CHROM BAN
  • [8] MORTON NE, 1956, AM J HUM GENET, V8, P80
  • [9] MORTON NE, 1955, AM J HUM GENET, V7, P183
  • [10] OTT J, 1974, AM J HUM GENET, V26, P558