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Nature Genetics|December 8, 1998
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairmentJ H Xia, C Y Liu, B S Tang, et al.Nature Genetics|January 31, 2006
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgarisFrances J D Smith, Alan D Irvine, Ana Terron-Kwiatkowski, et al.Nature Genetics|February 14, 2006
Rhythmic CLOCK-BMAL1 binding to multiple E-box motifs drives circadian Dbp transcription and chromatin transitionsJürgen A Ripperger, Ueli SchiblerNature Genetics|February 8, 2006
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humansSharlene Murdoch, Ugljesa Djuric, Batool Mazhar, et al.Nature Genetics|January 18, 2006
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndromeMira Kyttälä, Jonna Tallila, Riitta Salonen, et al.Nature Genetics|January 24, 2006
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathyAlbena Jordanova, Joy Irobi, Florian P Thomas, et al.Nature Genetics|January 24, 2006
Induction, suppression and requirement of RNA silencing pathways in virulent Agrobacterium tumefaciens infectionsPatrice Dunoyer, Christophe Himber, Olivier VoinnetNature Genetics|February 1, 1997
Complete inventory of the yeast ABC proteinsA Decottignies, A GoffeauNature Genetics|February 1, 1997
Functional transplant of megabase human immunoglobulin loci recapitulates human antibody response in miceM J Mendez, L L Green, J R Corvalan, et al.Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.Pageof 744