Paul P, Jagelman D G, Fazio V W, McGannon E
Department of Colorectal Surgery, Cleveland Clinic Foundation, Ohio 44195.
Dis Colon Rectum. 1990 Sep;33(9):740-4. doi: 10.1007/BF02052318.
A gene associated with the inherited syndrome, familial adenomatous polyposis (FAP), has been localized to the long arm of chromosome 5 near the 5q21-22 region, and markers that identify genetic polymorphisms near this locus are now available. The authors evaluated several of these markers for linkage to the FAP trait in 11 families entered in the Cleveland Clinic Polyposis Registry. The original probe that established linkage to the FAP locus (C11p11) has limited utility for family studies because of low heterozygosity and distance from the FAP gene. Other probes, however, should be useful for assessing FAP inheritance by restriction fragment length polymorphism analysis, for presymptomatic diagnosis of the disease.
一种与遗传性综合征——家族性腺瘤性息肉病(FAP)相关的基因已被定位到5号染色体长臂靠近5q21 - 22区域的位置,并且现在已有能够识别该基因座附近基因多态性的标记物。作者在克利夫兰诊所息肉病登记处登记的11个家族中评估了其中几种标记物与FAP性状的连锁关系。最初确定与FAP基因座连锁的探针(C11p11)由于杂合性低且与FAP基因距离较远,在家族研究中的用途有限。然而,其他探针应该可用于通过限制性片段长度多态性分析来评估FAP遗传情况,用于该疾病的症状前诊断。