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Nature Genetics|May 1, 1992
A novel GC-rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomesJ Giacalone, J Friedes, U FranckeNature Genetics|May 1, 1992
Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital developmentW Bruening, N Bardeesy, B L Silverman, et al.Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.Nature Genetics|July 1, 1992
Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAsG Jansen, M Mahadevan, C Amemiya, et al.Nature Genetics|August 1, 1992
Fragile X syndrome without CCG amplification has an FMR1 deletionA K Gedeon, E Baker, H Robinson, et al.Nature Genetics|August 1, 1992
A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloidM Mullan, F Crawford, K Axelman, et al.Nature Genetics|December 24, 2002
Mutations in NR4A2 associated with familial Parkinson diseaseWei-Dong Le, Pingyi Xu, Joseph Jankovic, et al.Nature Genetics|December 24, 2002
DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cellsMarie-France Robert, Steves Morin, Normand Beaulieu, et al.Nature Genetics|March 26, 2003
Erosion of the telomeric single-strand overhang at replicative senescenceSheila A Stewart, Ittai Ben-Porath, Vincent J Carey, et al.Nature Genetics|March 26, 2003
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humansChristopher S Carlson, Michael A Eberle, Mark J Rieder, et al.Pageof 744