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Nature Genetics|January 1, 1995
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instabilityB Liu, N C Nicolaides, S Markowitz, et al.Nature Genetics|January 1, 1993
The molecular basis of the human serum paraoxonase activity polymorphismR Humbert, D A Adler, C M Disteche, et al.Nature Genetics|March 26, 2002
Pbx1 inactivation disrupts pancreas development and in Ipf1-deficient mice promotes diabetes mellitusSeung K Kim, Licia Selleri, Joon S Lee, et al.Nature Genetics|April 10, 2002
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndromeGayle B Collin, Jan D Marshall, Akihiro Ikeda, et al.Nature Genetics|May 7, 2002
nagie oko, encoding a MAGUK-family protein, is essential for cellular patterning of the retinaXiangyun Wei, Jarema MalickiNature Genetics|May 7, 2002
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsyPatrick Cossette, Lidong Liu, Katéri Brisebois, et al.Nature Genetics|May 7, 2002
Suppression of the p53- or pRB-mediated G1 checkpoint is required for E2F-induced S-phase entryMarina Lomazzi, M Cristina Moroni, Michael R Jensen, et al.Nature Genetics|March 29, 2002
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like proteinChristopher J Ward, Marie C Hogan, Sandro Rossetti, et al.Nature Genetics|March 29, 2002
Molecular characterization of inter-telomere and intra-telomere mutations in human ALT cellsHelen Varley, Hilda A Pickett, Jennifer L Foxon, et al.Pageof 743