{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,13]],"date-time":"2025-12-13T07:01:36Z","timestamp":1765609296818},"reference-count":32,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2005,6,7]],"date-time":"2005-06-07T00:00:00Z","timestamp":1118102400000},"content-version":"vor","delay-in-days":4283,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1993,9,15]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Linkage studies on familial adenomatous polyposis (FAP) reported so far suggest that FAP is a genetically homogeneous disease. Recently, we found that the putative gene for Turcot syndrome, an apparently autosomal recessive clinical variant of FAP, is not allelic to FAP. Here we describe another family, segregating for an autosomal dominant disease clinically indistinguishable from FAP but genetically not linked to the APC locus, adding further evidence for the occurrence of non\u2010allelic heterogeneity of FA. These observations have implications to the linkage\u2010based genetic counselling of persons at risk for FAP especially when they are drawn from small families giving insufficient information. \u00a9 1993 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.1320470425","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T16:34:21Z","timestamp":1118507661000},"page":"563-567","source":"Crossref","is-referenced-by-count":24,"title":["Non\u2010allelic heterogeneity of familial adenomatous polyposis"],"prefix":"10.1002","volume":"47","author":[{"given":"Carli M. 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