LINKAGE STUDIES IN ITALIAN FAMILIES WITH FAMILIAL ADENOMATOUS POLYPOSIS

被引:6
作者
MARENI, C
STELLA, A
ORIGONE, P
SUSCA, F
MONTERA, MP
LONOCE, A
DELEON, MP
SASSATELLI, R
GENTILE, M
STRAFACE, A
CARUSO, ML
PALASCIANO, N
AJMAR, F
GUANTI, G
机构
[1] UNIV BARI,INST GENET,VIA AMENDOLA 165A,I-70126 BARI,ITALY
[2] UNIV GENOA,DEPT INTERNAL MED,I-16132 GENOA,ITALY
[3] IRCCS S DEBELLIS,CASTELLANZA,ITALY
[4] UNIV MODENA,INST MED PATHOL,I-41100 MODENA,ITALY
[5] INST BIOL & GENET,I-16132 GENOA,ITALY
[6] UNIV BARI,DEPT SURG 3,I-70126 BARI,ITALY
[7] UNIV BARI,DEPT SURG 1,I-70126 BARI,ITALY
关键词
D O I
10.1007/BF00217456
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Linkage analysis was performed on 188 subjects belonging to 18 Italian families segregating for familial adenomatous polyposis (FAP) using 7 polymorphic markers (5 restriction fragment length and 2 dinucleotide repeat polymorphisms) mapping in 5q21. A two-point linkage analysis performed with the LINKAGE program gave significant lod scores (> 3) between the Pi227, C11p11, YN5.64, YN5.48 probes and the discase, whereas the ECB27, CB83 and EF5.44 markers showed lower lod scores. Some 11 recombination events were identified from the analysis of 101 meioses. The best map that we could determine confirmed that reported in previous studies. The location of the new marker, CB83, lying between YN5.64 and YN5.48, remains imprecise. No genetic heterogeneity was detected, with all the families showing linkage for at least one of the probes. One 34-year-old individual having an affected haplotype was however classified as healthy after clinical examinations. The results confirm the applicability of the linkage approach for presymptomatic diagnosis of FAP.
引用
收藏
页码:545 / 550
页数:6
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