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 [J].
ARVEILER, B ;
ALEMBIK, Y ;
HANAUER, A ;
JACOBS, P ;
TRANEBJAERG, L ;
MIKKELSEN, M ;
PUISSANT, H ;
PIET, LL ;
MANDEL, JL .
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 [J].
BAKKER, E ;
BONTEN, EJ ;
DELANGE, LF ;
VEENEMA, H ;
MAJOORKRAKAUER, D ;
HOFKER, MH ;
VANOMMEN, GJB ;
PEARSON, PL .
JOURNAL OF MEDICAL GENETICS, 1986, 23 (06) :573-580
[3]   ABNORMAL PROTEODERMATAN SULFATE IN 3 PATIENTS WITH COFFIN-LOWRY SYNDROME [J].
BECK, M ;
GLOSSL, J ;
RUTER, R ;
KRESSE, H .
PEDIATRIC RESEARCH, 1983, 17 (11) :926-929
[4]   LOCALIZATION OF XP21 MEIOTIC EXCHANGE POINTS IN DUCHENNE MUSCULAR-DYSTROPHY FAMILIES [J].
BERTELSON, CJ ;
BARTLEY, JA ;
MONACO, AP ;
COLLETTIFEENER, C ;
FISCHBECK, K ;
KUNKEL, LM .
JOURNAL OF MEDICAL GENETICS, 1986, 23 (06) :531-537
[5]   MENTAL RETARDATION WITH OSTEOCARTILAGINOUS ANOMALIES [J].
COFFIN, GS ;
SIRIS, E ;
WEGIENKA, LC .
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 [J].
DRAYNA, D ;
WHITE, R .
SCIENCE, 1985, 230 (4727) :753-758
[8]   COFFIN SYNDROME [J].
FRYNS, JP ;
VINKEN, L ;
VANDENBERGHE, H .
HUMAN GENETICS, 1977, 36 (03) :271-276
[9]   THE COFFIN-LOWRY SYNDROME - A STUDY OF 2 NEW INDEX PATIENTS AND THEIR FAMILIES [J].
HASPESLAGH, M ;
FRYNS, JP ;
BEUSEN, L ;
VANDESSEL, F ;
VINKEN, L ;
MOENS, E ;
VANDENBERGHE, H .
EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (02) :82-86
[10]  
HUNTER AGW, 1982, CLIN GENET, V21, P321