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The New England Journal of Medicine|May 26, 1988
Prevalence of hemochromatosis among 11,065 presumably healthy blood donorsC Q Edwards, L M Griffen, D Goldgar, et al.International Journal of Cancer|December 20, 1995
Risk modifiers in carriers of BRCA1 mutationsS A Narod, D Goldgar, L Cannon-Albright, et al.Journal of the American Academy of Dermatology|March 1, 1989
The dysplastic melanocytic nevus: a prevalent lesion that correlates poorly with clinical phenotypeM Piepkorn, L J Meyer, D Goldgar, et al.Science (New York, N.Y.)|May 29, 1987
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17D Barker, E Wright, K Nguyen, et al.Journal of Medical Genetics|September 1, 1987
A genomic search for linkage of neurofibromatosis to RFLPsD Barker, E Wright, K Nguyen, et al.American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.Lancet (London, England)|June 15, 1996
Germline BRCA1 185delAG mutations in Jewish women with breast cancerK Offit, T Gilewski, P McGuire, et al.Genomics|December 1, 1987
Tightly linked markers for the neurofibromatosis type 1 geneR White, Y Nakamura, P O'Connell, et al.Breast Cancer Research and Treatment|August 19, 2011
Prospective study of breast cancer risk for mutation negative women from BRCA1 or BRCA2 mutation positive familiesS L Harvey, R L Milne, S A McLachlan, et al.British Journal of Cancer|June 13, 2013
Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancerD R Barnes, D Barrowdale, J Beesley, et al.Pageof 4