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Nature Genetics|March 31, 2000
Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouseK Lindblad-Toh, E Winchester, M J Daly, et al.Nature Genetics|March 31, 2000
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formationI Satokata, L Ma, H Ohshima, et al.Nature Genetics|March 31, 2000
Heterogeneous mutation processes in human microsatellite DNA sequencesH EllegrenNature Genetics|March 31, 2000
Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged miceD Pennisi, J Gardner, D Chambers, et al.Nature Genetics|March 31, 2000
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosisM P Bulman, K Kusumi, T M Frayling, et al.Nature Genetics|May 10, 2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switchB Bielinska, S M Blaydes, K Buiting, et al.Nature Genetics|October 3, 1999
Early specification of limb muscle precursor cells by the homeobox gene Lbx1hK Schäfer, T BraunNature Genetics|October 3, 1999
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8S Ranta, Y Zhang, B Ross, et al.Nature Genetics|October 3, 1999
Loss of Cul1 results in early embryonic lethality and dysregulation of cyclin EM J Dealy, K V Nguyen, J Lo, et al.Nature Genetics|November 5, 1999
Diverse and dynamic functions of the Sir silencing complexL GuarentePageof 744