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Nature Genetics|July 12, 2005
Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cellsMichael Weber, Jonathan J Davies, David Wittig, et al.Nature Genetics|August 24, 2005
Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesisOlivier Gribouval, Marie Gonzales, Thomas Neuhaus, et al.Nature Genetics|August 24, 2005
The t complex-encoded GTPase-activating protein Tagap1 acts as a transmission ratio distorter in miceHermann Bauer, Jürgen Willert, Birgit Koschorz, et al.Nature Genetics|September 20, 2005
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesAlison J Ross, Helen May-Simera, Erica R Eichers, et al.Nature Genetics|September 20, 2005
Germline mutations in HRAS proto-oncogene cause Costello syndromeYoko Aoki, Tetsuya Niihori, Hiroshi Kawame, et al.Nature Genetics|September 6, 2005
Genomic alterations in cultured human embryonic stem cellsAnirban Maitra, Dan E Arking, Narayan Shivapurkar, et al.Nature Genetics|September 6, 2005
Identification of mutations in CUL7 in 3-M syndromeCéline Huber, Dora Dias-Santagata, Anna Glaser, et al.Nature Genetics|September 13, 2005
A variable number of tandem repeats polymorphism in an E2F-1 binding element in the 5' flanking region of SMYD3 is a risk factor for human cancersMasataka Tsuge, Ryuji Hamamoto, Fabio Pittella Silva, et al.Nature Genetics|September 13, 2005
Genome-scale profiling of histone H3.3 replacement patternsYoshiko Mito, Jorja G Henikoff, Steven HenikoffNature Genetics|July 19, 2005
Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmyGábor Zsurka, Yevgenia Kraytsberg, Tatiana Kudina, et al.Pageof 745