A PRIMARY LINKAGE MAP OF THE HUMAN CHROMOSOME-11Q22-23 REGION

被引:32
作者
CHARMLEY, P
FOROUD, T
WEI, S
CONCANNON, P
WEEKS, DE
LANGE, K
GATTI, RA
机构
[1] UNIV CALIF LOS ANGELES, SCH MED, DEPT PATHOL, LOS ANGELES, CA 90024 USA
[2] UNIV CALIF LOS ANGELES, SCH MED, DEPT MICROBIOL & IMMUNOL, LOS ANGELES, CA 90024 USA
[3] UNIV CALIF LOS ANGELES, SCH MED, DEPT BIOMATH, LOS ANGELES, CA 90024 USA
[4] VIRGINIA MASON RES CTR, SEATTLE, WA 98101 USA
[5] COLUMBIA UNIV, NEW YORK, NY 10027 USA
[6] NEW YORK STATE PSYCHIAT INST & HOSP, NEW YORK, NY 10032 USA
关键词
D O I
10.1016/0888-7543(90)90572-C
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
We have constructed a genetic map of the human chromosomal region 11q22-23 by multipoint linkage analysis of 13 DNA polymorphisms that we have condensed into eight loci. An analysis for linkage disequilibrium between tightly linked probe/enzyme systems allows us to make specific recommendations for future DNA typing at these loci. The resulting sex-averaged multipoint map spans approximately 80 cM and differs considerably from previously reported genetic maps of this region. Our mathematically derived "most likely order" of the markers is compatible with physical mapping data using somatic cell hybrids. The known localizations of at least 14 functional genes and several disease loci to 11q22-23, including ataxia telangiectasia, make the mapping of this region especially relevant to studies of disease pathogenesis. © 1990.
引用
收藏
页码:316 / 323
页数:8
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