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Revue Neurologique|November 23, 2007
[Phenotype-genotype study in 154 French NF2 mutation carriers]L Demange, C De Moncuit, G Thomas, et al.Journal of Medical Genetics|June 5, 2001
Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinomaS Olschwang, C Boisson, G ThomasHuman Genetics|September 1, 1992
Frequent polymorphism in the 13th exon of the adenomatous polyposis coli geneS Olschwang, P Laurent-Puig, B Thuille, et al.European Journal of Human Genetics : EJHG|January 1, 1995
DNA-based presymptomatic diagnosis for the von Hippel-Lindau disease by linkage analysisS Olschwang, C Boisson, S Richard, et al.Cytogenetics and Cell Genetics|January 1, 1994
Mapping of 18 probes on human chromosome 18 using single- and double-color FISHM Muleris, F Apiou, S Olschwang, et al.European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ECP)|April 20, 2000
Germline mutation and genome instabilityS OlschwangAmerican Journal of Medical Genetics|May 8, 1995
High resolution genetic map of the adenomatous polyposis coli gene (APC) regionS Olschwang, P Laurent-Puig, T Melot, et al.American Journal of Human Genetics|February 1, 1993
Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) geneS Olschwang, P Laurent-Puig, J Groden, et al.Pageof 424