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Nature Genetics|October 1, 2003
Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosisMichael L Woodruff, Zhongyan Wang, Hae Yun Chung, et al.Nature Genetics|October 1, 2003
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndromeRaymonda Varon, Rebecca Gooding, Christina Steglich, et al.Nature Genetics|November 5, 2003
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)Koki Yamada, Caroline Andrews, Wai-Man Chan, et al.Nature Genetics|August 19, 2003
Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in micePierre L Roubertoux, Frans Sluyter, Michèle Carlier, et al.Nature Genetics|August 19, 2003
Cyclin-dependent kinase 2 is essential for meiosis but not for mitotic cell division in miceSagrario Ortega, Ignacio Prieto, Junko Odajima, et al.Nature Genetics|September 6, 2003
Mutations in NHLRC1 cause progressive myoclonus epilepsyElayne M Chan, Edwin J Young, Leonarda Ianzano, et al.Nature Genetics|November 1, 1992
X inactivation in mammalian testis is correlated with inactive X-specific transcriptionC Richler, H Soreq, J WahrmanNature Genetics|November 1, 1992
Cloning of the alpha-adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplificationS A Taylor, R G Snell, A Buckler, et al.Nature Genetics|June 5, 2003
Mutations in proto-oncogene GFI1 cause human neutropenia and target ELA2Richard E Person, Feng-Qian Li, Zhijun Duan, et al.Nature Genetics|September 1, 1992
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyC Wijmenga, J E Hewitt, L A Sandkuijl, et al.Pageof 742