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Nature Genetics|August 1, 1994
Identification and characterization of the gene causing type 1 spinocerebellar ataxiaS Banfi, A Servadio, M Y Chung, et al.Nature Genetics|December 1, 1994
Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndromeP T Brook-Carter, B Peral, C J Ward, et al.Nature Genetics|December 1, 1994
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyB H Weber, G Vogt, R C Pruett, et al.Nature Genetics|December 1, 1994
The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic associationM Pigg, S Jagell, A Sillén, et al.Nature Genetics|December 1, 1994
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.Nature Genetics|December 1, 1994
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten familiesL S Friedman, E A Ostermeyer, C I Szabo, et al.Nature Genetics|June 1, 1994
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinismD Durham-Pierre, J M Gardner, Y Nakatsu, et al.Nature Genetics|June 1, 1994
Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin geneB Glaser, K C Chiu, R Anker, et al.Nature Genetics|June 1, 1994
Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophyB C Broughton, H Steingrimsdottir, C A Weber, et al.Nature Genetics|July 1, 1994
Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mappingP W Reed, J L Davies, J B Copeman, et al.Pageof 743