DNA MARKER D11S384 SHOWS ZERO RECOMBINATION WITH THE ATAXIA-TELANGIECTASIA LOCUS IN NORTH-AMERICAN FAMILIES

被引:2
作者
LENCH, NJ
ATHMA, P
OTTAIANO, A
SRIBNEY, WM
HIGHSMITH, E
SWIFT, M
机构
[1] NEW YORK MED COLL,DIV HUMAN MOLEC GENET,VALHALLA,NY 10595
[2] NEW YORK MED COLL,INST GENET ANAL COMMON DIS,VALHALLA,NY 10595
[3] NEW YORK MED COLL,DEPT PEDIAT,VALHALLA,NY 10595
[4] APPL TECHNOL GENET CORP,MALVERN,PA
关键词
D O I
10.1080/09553009414551881
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
At the genetic locus D11S384, one probe detects a Taq1 RFLP and another detects a RFMP. In 52 pedigrees of North American A-T patients, parental haplotypes based on these two bi-allelic systems have a heterozygosity of 0.69 and a PIC of 0.64. No recombinant events between D11S384 and the A-T locus were detected in the 43 pedigrees in which this marker locus was informative.
引用
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页码:S67 / S69
页数:3
相关论文
共 11 条
[1]  
FOROUD T, 1991, AM J HUM GENET, V49, P1263
[2]  
GATTI RA, 1988, NATURE, V336, P557
[3]  
GRAY MR, 1992, AM J HUM GENET, V50, P331
[4]   GENETIC COMPLEMENTATION ANALYSIS OF ATAXIA TELANGIECTASIA AND NIJMEGEN BREAKAGE SYNDROME - A SURVEY OF 50 PATIENTS [J].
JASPERS, NGJ ;
GATTI, RA ;
BAAN, C ;
LINSSEN, PCML ;
BOOTSMA, D .
CYTOGENETICS AND CELL GENETICS, 1988, 49 (04) :259-263
[5]   ISOLATION AND MAPPING OF A POLYMORPHIC DNA-SEQUENCE (CJ52.193) ON CHROMOSOME-11 [J].
JULIER, C ;
GILL, J ;
NAKAMURA, Y ;
LATHROP, GM ;
LALOUEL, JM ;
WHITE, R .
NUCLEIC ACIDS RESEARCH, 1989, 17 (22) :9501-9501
[6]  
LATHROP GM, 1985, AM J HUM GENET, V37, P482
[7]  
LENCH NJ, 1991, CYTOGENET CELL GENET, V58, P1965
[8]  
LENCH NJ, 1994, UNPUB DETECTION RFMP
[9]  
MCCONVILLE CM, 1993, HUM MOL GENET, V2, P969
[10]  
SANAL O, 1990, AM J HUM GENET, V47, P860