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Nature Genetics|April 1, 1996
A locus for bipolar affective disorder on chromosome 4pD H Blackwood, L He, S W Morris, et al.Nature Genetics|April 1, 1996
Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23N B Freimer, V I Reus, M A Escamilla, et al.Nature Genetics|April 1, 1996
Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpointA Schulze, C Hansen, N E Skakkebaek, et al.Nature Genetics|October 1, 1996
The genetical archaeology of the human genomeA von Haeseler, A Sajantila, S PääboNature Genetics|October 1, 1996
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMKD B Simon, F E Karet, J Rodriguez-Soriano, et al.Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.Nature Genetics|October 1, 1996
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndromeI Hatada, H Ohashi, Y Fukushima, et al.Nature Genetics|October 1, 1996
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesG A Bellus, K Gaudenz, E H Zackai, et al.Nature Genetics|October 1, 1996
Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody diseaseA Odermatt, P E Taschner, V K Khanna, et al.Nature Genetics|October 1, 1996
Selective ablation of differentiated cells permits isolation of embryonic stem cell lines from murine embryos with a non-permissive genetic backgroundJ McWhir, A E Schnieke, R Ansell, et al.Pageof 742