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pubmed-article:9087571pubmed:abstractTextThe basal cell nevus syndrome (Gorlin syndrome) is characterized by multiple basal cell carcinomas and diverse developmental defects. The gene responsible for this syndrome has been mapped previously to a 2 cM interval between D9S196 and D9S 180 at 9q22.3, and very recently mutations of a candidate gene in this region--the human homolog of the Drosophila patched gene have been identified. We report here on physical mapping studies integrating a contig of yeast artificial chromosomes and bacterial artificial chromosomes with a long-range map spanning approximately 5 Mb between the recombination-determined flanking markers. Six genes have been mapped to this interval.lld:pubmed
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pubmed-article:9087571pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:9087571pubmed:year1997lld:pubmed
pubmed-article:9087571pubmed:articleTitlePhysical mapping of the 5 Mb D9S196-D9S180 interval harboring the basal cell nevus syndrome gene and localization of six genes in this region.lld:pubmed
pubmed-article:9087571pubmed:affiliationDepartment of Dermatology, San Francisco General Hospital, California 94110, USA.lld:pubmed
pubmed-article:9087571pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9087571pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:9087571pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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