学术探索
学术期刊
新闻热点
数据分析
智能评审

PROBABLE LOCALIZATION OF THE COFFIN-LOWRY LOCUS IN XP22.2-P22.1 BY MULTIPOINT LINKAGE ANALYSIS

被引：46
作者：
HANAUER, A
ALEMBIK, Y
GILGENKRANTZ, S
MUJICA, P
NIVELONCHEVALLIER, A
PEMBREY, ME
YOUNG, ID
MANDEL, JL
机构：
[1] INSERM,INSERM,U184,11 RUE HUMAN,F-67200 STRASBOURG,FRANCE
[2] INSERM,CNRS,GENET MOLEC EUCARYOTES LAB,F-67200 STRASBOURG,FRANCE
[3] CTR TRANSFUS SANGUINE,NANCY,ENGLAND
[4] HOP ENFANTS,CTR GENET,DIJON,ENGLAND
[5] INST CHILD HLTH,DEPT PAEDIAT GENET,LONDON WC1N 1EH,ENGLAND
[6] UNIV LEICESTER,DEPT CHILD HLTH,LEICESTER LE1 7RH,ENGLAND
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 30卷 / 1-2期
关键词：
D O I：
10.1002/ajmg.1320300154
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：523 / 530
页数：8
相关论文
共 17 条
  • [1] LINKAGE ANALYSIS SUGGESTS AT LEAST 2 LOCI FOR X-LINKED NON-SPECIFIC MENTAL-RETARDATION
    ARVEILER, B
    ALEMBIK, Y
    HANAUER, A
    JACOBS, P
    TRANEBJAERG, L
    MIKKELSEN, M
    PUISSANT, H
    PIET, LL
    MANDEL, JL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 473 - 483
  • [2] DNA PROBE ANALYSIS FOR CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY - A STANDARD DIAGNOSTIC PROCEDURE
    BAKKER, E
    BONTEN, EJ
    DELANGE, LF
    VEENEMA, H
    MAJOORKRAKAUER, D
    HOFKER, MH
    VANOMMEN, GJB
    PEARSON, PL
    [J]. JOURNAL OF MEDICAL GENETICS, 1986, 23 (06) : 573 - 580
  • [3] ABNORMAL PROTEODERMATAN SULFATE IN 3 PATIENTS WITH COFFIN-LOWRY SYNDROME
    BECK, M
    GLOSSL, J
    RUTER, R
    KRESSE, H
    [J]. PEDIATRIC RESEARCH, 1983, 17 (11) : 926 - 929
  • [4] LOCALIZATION OF XP21 MEIOTIC EXCHANGE POINTS IN DUCHENNE MUSCULAR-DYSTROPHY FAMILIES
    BERTELSON, CJ
    BARTLEY, JA
    MONACO, AP
    COLLETTIFEENER, C
    FISCHBECK, K
    KUNKEL, LM
    [J]. JOURNAL OF MEDICAL GENETICS, 1986, 23 (06) : 531 - 537
  • [5] MENTAL RETARDATION WITH OSTEOCARTILAGINOUS ANOMALIES
    COFFIN, GS
    SIRIS, E
    WEGIENKA, LC
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1966, 112 (03): : 205 - &
  • [6] COLLACOTT RA, 1987, J MENT DEFIC RES, V31, P199
  • [7] THE GENETIC-LINKAGE MAP OF THE HUMAN X-CHROMOSOME
    DRAYNA, D
    WHITE, R
    [J]. SCIENCE, 1985, 230 (4727) : 753 - 758
  • [8] COFFIN SYNDROME
    FRYNS, JP
    VINKEN, L
    VANDENBERGHE, H
    [J]. HUMAN GENETICS, 1977, 36 (03) : 271 - 276
  • [9] THE COFFIN-LOWRY SYNDROME - A STUDY OF 2 NEW INDEX PATIENTS AND THEIR FAMILIES
    HASPESLAGH, M
    FRYNS, JP
    BEUSEN, L
    VANDESSEL, F
    VINKEN, L
    MOENS, E
    VANDENBERGHE, H
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (02) : 82 - 86
  • [10] HUNTER AGW, 1982, CLIN GENET, V21, P321
12