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Nature Genetics|November 1, 1995
Targeted mutation in the Fas gene causes hyperplasia in peripheral lymphoid organs and liverM Adachi, S Suematsu, T Kondo, et al.Nature Genetics|November 1, 1995
An international two-stage genome-wide search for schizophrenia susceptibility genesH W Moises, L Yang, H Kristbjarnarson, et al.Nature Genetics|November 1, 1995
Contribution of the FMR1 gene mutation to human intellectual dysfunctionA L Reiss, L S Freund, T L Baumgardner, et al.Nature Genetics|August 1, 1993
Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase geneW Guo, K Worley, V Adams, et al.Nature Genetics|December 1, 1993
Mapping, cloning and genetic characterization of the region containing the Wilson disease geneK Petrukhin, S G Fischer, M Pirastu, et al.Nature Genetics|December 1, 1993
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease geneR E Tanzi, K Petrukhin, I Chernov, et al.Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.Nature Genetics|December 1, 1993
Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structureT Meitinger, A Meindl, P Bork, et al.Nature Genetics|December 1, 1993
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14qT G Nygaard, K C Wilhelmsen, N J Risch, et al.Nature Genetics|December 1, 1993
Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.Pageof 744