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Nature Genetics|October 31, 2001
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaX Zhao, D Alvarado, S Rainier, et al.Nature Genetics|October 31, 2001
Population genetic structure of variable drug responseJ F Wilson, M E Weale, A C Smith, et al.Nature Genetics|January 26, 2002
Inflammatory reactions and severe neutropenia in mice lacking the transcriptional repressor Gfi1Holger Karsunky, Hui Zeng, Thorsten Schmidt, et al.Nature Genetics|January 31, 2002
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesisBruce J Herron, Weining Lu, Cherie Rao, et al.Nature Genetics|January 31, 2002
Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumorsNada Al-Tassan, Nikolas H Chmiel, Julie Maynard, et al.Nature Genetics|January 19, 2002
Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasiaCornelius F Boerkoel, Hiroshi Takashima, Joy John, et al.Nature Genetics|January 19, 2002
Chromosomal effects of adeno-associated virus vector integrationDaniel G Miller, Elizabeth A Rutledge, David W RussellNature Genetics|October 16, 2001
Mutant protein in Huntington disease is resistant to proteolysis in affected brainR B Dyer, C T McMurrayNature Genetics|October 16, 2001
Replication validity of genetic association studiesJ P Ioannidis, E E Ntzani, T A Trikalinos, et al.Nature Genetics|March 30, 2001
Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung diseaseN Wakamatsu, Y Yamada, K Yamada, et al.Pageof 744