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Nature Genetics|May 13, 1999
Loss of Cdk4 expression causes insulin-deficient diabetes and Cdk4 activation results in beta-islet cell hyperplasiaS G Rane, P Dubus, R V Mettus, et al.Nature Genetics|May 13, 1999
Sequence variation in the human angiotensin converting enzymeM J Rieder, S L Taylor, A G Clark, et al.Nature Genetics|May 13, 1999
Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinaseR Shinkura, K Kitada, F Matsuda, et al.Nature Genetics|May 13, 1999
DNA sequence variation in a non-coding region of low recombination on the human X chromosomeH Kaessmann, F Heissig, A von Haeseler, et al.Nature Genetics|May 13, 1999
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndromeS Kitao, A Shimamoto, M Goto, et al.Nature Genetics|May 13, 1999
Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotypeT Hayashi, A G Motulsky, S S DeebNature Genetics|December 30, 1999
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type IP Momeni, G Glöckner, O Schmidt, et al.Nature Genetics|December 30, 1999
DNA methyltransferase Dnmt1 associates with histone deacetylase activityF Fuks, W A Burgers, A Brehm, et al.Nature Genetics|November 4, 2000
Mining the human genome using microarrays of open reading framesS G Penn, D R Rank, D K Hanzel, et al.Nature Genetics|November 4, 2000
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23Pageof 744