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Human Mutation|December 29, 1999
PAHdb: a locus-specific knowledgebaseC R Scriver, P J Waters, C Sarkissian, et al.Human Mutation|December 29, 1999
p53 website and analysis of p53 gene mutations in human cancer: forging a link between epidemiology and carcinogenesisT Soussi, K Dehouche, C BéroudHuman Mutation|December 29, 1999
Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiencyE Mayatepek, J Nezu, I Tamai, et al.Human Mutation|December 29, 1999
Quality control in the discovery, reporting, and recording of genomic variationR G Cotton, O HoraitisHuman Mutation|December 29, 1999
Ethical guideposts for allelic variation databasesB M Knoppers, C M LabergeHuman Mutation|December 29, 1999
Use of molecular variation in the NCBI dbSNP databaseS T Sherry, M Ward, K SirotkinHuman Mutation|December 29, 1999
Somatic mosaicism in von Hippel-Lindau DiseaseA Murgia, M Martella, C Vinanzi, et al.Human Mutation|April 24, 1999
A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia. Mutations in brief no. 122. OnlineG Grigelioniené, L Hagenäs, O Eklöf, et al.Human Mutation|April 24, 1999
Detection of four novel mutations in the iduronate-2-sulfatase gene. Mutations in brief no. 123. OnlineN Balzano, G R Villani, M Grosso, et al.Pageof 583