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In this report we present a series of Australian PJS cases, which suggest that mutations in the STK11 gene do not account for many families or patients without a family history. The most likely explanation is either the presence of another susceptibility gene or genetic mosaicism in the non\u2010familial patients.<\/jats:p>","DOI":"10.1034\/j.1399-0004.2002.620405.x","type":"journal-article","created":{"date-parts":[[2003,3,11]],"date-time":"2003-03-11T11:30:26Z","timestamp":1047382226000},"page":"282-287","source":"Crossref","is-referenced-by-count":51,"title":["Mutation analysis of the STK11\/LKB1 gene and clinical characteristics of an Australian series of Peutz\u2013Jeghers syndrome 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