Search Results - Mæhle, L.O

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    A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing

    A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing by Dørum, A, Møller, P, Kamsteeg, E.J, Scheffer, H, Burton, M, Heimdal, K.R, Mæhle, L.O, Hovig, E, Tropé, C.G, van der Hout, A.H, van der Meulen, M.A, Buys, C.H.C.M, te Meerman, G.J

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