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Nature Genetics|November 5, 1999
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndromeJ Marcelino, J D Carpten, W M Suwairi, et al.Nature Genetics|November 5, 1999
Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitusM T Malecki, U S Jhala, A Antonellis, et al.Nature Genetics|November 5, 1999
Mammalian (cytosine-5) methyltransferases cause genomic DNA methylation and lethality in DrosophilaF Lyko, B H Ramsahoye, H Kashevsky, et al.Nature Genetics|August 10, 2000
EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndromeM Delépine, M Nicolino, T Barrett, et al.Nature Genetics|August 10, 2000
Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees. Australian Breast Cancer Family StudyG A Huttley, S Easteal, M C Southey, et al.Nature Genetics|August 10, 2000
Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasiaK Suzuki, D Hu, T Bustos, et al.Nature Genetics|July 3, 1999
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosaE A Pierce, T Quinn, T Meehan, et al.Nature Genetics|July 3, 1999
Regulation of anterior/posterior patterning of the axial skeleton by growth/differentiation factor 11A C McPherron, A M Lawler, S J LeeNature Genetics|July 3, 1999
Mutations in the gene encoding 3 beta-hydroxysteroid-delta 8, delta 7-isomerase cause X-linked dominant Conradi-Hünermann syndromeN Braverman, P Lin, F F Moebius, et al.Nature Genetics|July 3, 1999
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporterJ C Fleming, E Tartaglini, M P Steinkamp, et al.Pageof 744