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Nature Genetics|December 1, 1992
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expressionB M Cattanach, J A Barr, E P Evans, et al.Nature Genetics|December 1, 1992
Telomere-associated chromosome fragmentation: applications in genome manipulation and analysisC J Farr, M Stevanovic, E J Thomson, et al.Nature Genetics|December 1, 1992
Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1AL J Valentijn, F Baas, R A Wolterman, et al.Nature Genetics|December 1, 1992
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophyA R La Spada, D B Roling, A E Harding, et al.Nature Genetics|December 1, 1992
Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosomeI del Castillo, M Cohen-Salmon, S Blanchard, et al.Nature Genetics|December 1, 1992
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brainN W Soong, D R Hinton, G Cortopassi, et al.Nature Genetics|April 22, 2003
Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosisMartina Muckenthaler, Cindy N Roy, Angel O Custodio, et al.Nature Genetics|August 5, 2003
Trans-acting regulatory variation in Saccharomyces cerevisiae and the role of transcription factorsGaël Yvert, Rachel B Brem, Jacqueline Whittle, et al.Nature Genetics|August 12, 2003
Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing lossKonrad Noben-Trauth, Qing Yin Zheng, Kenneth R JohnsonNature Genetics|April 1, 1992
Human CCAAT displacement protein is homologous to the Drosophila homeoprotein, cutE J Neufeld, D G Skalnik, P M Lievens, et al.Pageof 744