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Faglig rapport 2006 - Helse Vest

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27Rudkin TM, Hamel N, Galvez M, Hogervorst F, Gille JJ, Møller P, Apold J, Foulkes WD"The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype studyin different populations."BMC Med Genet. <strong>2006</strong>;7:15PMID: 16509964<strong>Faglig</strong>e retningslinjerMetodebok arvelig kreft, <strong>2006</strong>

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