Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panel

被引:27
作者
Budarf, ML
Eckman, B
Michaud, D
McDonald, T
Gavigan, S
Buetow, KH
Tatsumura, Y
Liu, ZG
Hilliard, C
Driscoll, D
Goldmuntz, E
Meese, E
Zwarthoff, EC
Williams, S
McDermid, H
Dumanski, JP
Biegel, J
Bell, CJ
Emanuel, BS
机构
[1] CHILDRENS HOSP,DIV HUMAN GENET & MOLEC BIOL,PHILADELPHIA,PA 19104
[2] FOX CHASE CANC CTR,DIV POPULAT SCI,PHILADELPHIA,PA 19111
[3] UNIV SAARBRUCKEN,DEPT HUMAN GENET,SAARBRUCKEN,GERMANY
[4] ERASMUS UNIV ROTTERDAM,INST PATHOL,ROTTERDAM,NETHERLANDS
[5] UNIV ALBERTA,DEPT BIOL SCI,EDMONTON,AB,CANADA
[6] KAROLINSKA HOSP,DEPT MOLEC MED,CLIN GENET UNIT,S-17176 STOCKHOLM,SWEDEN
关键词
DINUCLEOTIDE REPEAT POLYMORPHISM; CHRONIC MYELOGENOUS LEUKEMIA; EWING SARCOMA BREAKPOINT; CARDIO-FACIAL SYNDROME; GENETIC-LINKAGE MAP; V-LAMBDA GENE; DIGEORGE SYNDROME; DNA MARKERS; STIMULATING FACTOR; INHIBITORY FACTOR;
D O I
10.1006/geno.1996.0358
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A somatic cell hybrid panel, consisting of 25 cell lines, has been developed to localize loci subregionally on chromosome 22. Over 300 markers in the form of STSs or hybridization probes have been assigned to one of 24 unique regions or ''bins'' using this panel. This ordered collection of markers will aid in the assembly of physical maps and contigs of chromosome 22 and assist in positional cloning of disease loci mapped to chromosome 22. (C) 1996 academic Press, Inc.
引用
收藏
页码:275 / 288
页数:14
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