Search Results - "van Leeuwen, Inge"

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    Mutant BRCA1 alleles transmission: Different approaches and different biases by de la Hoya, Miguel, Meijers‐Heijboer, Hanne, Fernández, Juan Manuel, Díez, Orland, Osorio, Ana, Alonso, Carmen, van Leeuwen, Inge, Díaz‐Rubio, Eduardo, Cornelisse, Cees, Benítez, Javier, Devilee, Peter, Caldés, Trinidad

    Published in International journal of cancer (01-01-2005)
    “…Recently, a non‐random transmission of BRCA1 mutant alleles to the off‐spring of carriers has been suggested. If confirmed by further studies, the finding will…”
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    Journal Article
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    Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis by Fodde, R, van der Luijt, R, Wijnen, J, Tops, C, van der Klift, H, van Leeuwen-Cornelisse, I, Griffioen, G, Vasen, H, Khan, P M

    Published in Genomics (San Diego, Calif.) (01-08-1992)
    “…Familial adenomatous polyposis (FAP) is a dominantly inherited condition predisposing to colorectal cancer. The recent isolation of the responsible gene…”
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    Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markers by Skraastad, M I, Verwest, A, Bakker, E, Vegter-van der Vlis, M, van Leeuwen-Cornelisse, I, Roos, R A, Pearson, P L, van Ommen, G J

    Published in American journal of medical genetics (01-05-1991)
    “…Presymptomatic, testing, prenatal diagnosis, or exclusion testing are now available for persons at risk for Huntington disease. These tests will reduce…”
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    Genetic evidence that Turcot syndrome is not allelic to familial adenomatous polyposis by Tops, C M, Vasen, H F, van Berge Henegouwen, G, Simoons, P P, van de Klift, H M, van Leeuwen, S J, Breukel, C, Fodde, R, den Hartog Jager, F C, Nagengast, F M

    Published in American journal of medical genetics (15-07-1992)
    “…Turcot syndrome (TS) is a rare genetic disease in which brain tumors occur in association with colonic polyposis. Since Turcot's original description in 1959,…”
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