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
[11]   COFFIN-LOWRY SYNDROME IN AN AFRO-AMERICAN FAMILY [J].
KOUSSEFF, BG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 11 (03) :373-375
[12]  
LATHROP GM, 1985, AM J HUM GENET, V37, P482
[13]   NEW DOMINANT GENE MENTAL RETARDATION SYNDROME - ASSOCIATION WITH SMALL STATURE, TAPERING FINGERS, CHARACTERISTIC FACIES, AND POSSIBLE HYDROCEPHALUS [J].
LOWRY, B ;
MILLER, JR ;
FRASER, FC .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1971, 121 (06) :496-&
[14]  
MCKUSICK VA, 1983, MENDELIAN INHERITANC, P1000
[15]   CHARACTERIZATION OF A SET OF X-LINKED SEQUENCES AND OF A PANEL OF SOMATIC-CELL HYBRIDS USEFUL FOR THE REGIONAL MAPPING OF THE HUMAN X-CHROMOSOME [J].
OBERLE, I ;
CAMERINO, G ;
KLOEPFER, C ;
MOISAN, JP ;
GRZESCHIK, KH ;
HELLKUHL, B ;
HORSCAYLA, MC ;
VANCONG, N ;
WEIL, D ;
MANDEL, JL .
HUMAN GENETICS, 1986, 72 (01) :43-49
[16]   MENTAL-RETARDATION, ABNORMAL FINGERS, AND SKELETAL ANOMALIES - COFFINS SYNDROME [J].
PROCOPIS, PG ;
TURNER, B .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1972, 124 (02) :258-&
[17]  
WILICHOWSKI E, 1987, HUM GENET, V75, P32