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Nature Genetics|October 3, 1999
Mre11 and Ku70 interact in somatic cells, but are differentially expressed in early meiosisW Goedecke, M Eijpe, H H Offenberg, et al.Nature Genetics|October 3, 1999
Genome-wide mapping with biallelic markers in Arabidopsis thalianaR J Cho, M Mindrinos, D R Richards, et al.Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.Nature Genetics|October 3, 1999
Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic developmentJ A Piedrahita, B Oetama, G D Bennett, et al.Nature Genetics|October 3, 1999
Susceptibility to testicular germ-cell tumours in a 129.MOLF-Chr 19 chromosome substitution strainA Matin, G B Collin, Y Asada, et al.Nature Genetics|March 10, 2001
SPTLC1 is mutated in hereditary sensory neuropathy, type 1K Bejaoui, C Wu, M D Scheffler, et al.Nature Genetics|March 10, 2001
Recombinational DNA double-strand breaks in mice precede synapsisS K Mahadevaiah, J M Turner, F Baudat, et al.Nature Genetics|March 10, 2001
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signalingR Döffinger, A Smahi, C Bessia, et al.Nature Genetics|March 10, 2001
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1L A Jerome, V E PapaioannouNature Genetics|March 10, 2001
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in miceR Z Chen, S Akbarian, M Tudor, et al.Pageof 745