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Nature Genetics|December 1, 1994
Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancerA Hemminki, P Peltomäki, J P Mecklin, et al.Nature Genetics|March 1, 1995
Gamete-specific methylation correlates with imprinting of the murine Xist geneM Ariel, E Robinson, J R McCarrey, et al.Nature Genetics|March 1, 1995
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3P L Tavormina, R Shiang, L M Thompson, et al.Nature Genetics|October 20, 2009
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosusVesela Gateva, Johanna K Sandling, Geoff Hom, et al.Nature Genetics|February 9, 2010
Common variants near TERC are associated with mean telomere lengthVeryan Codd, Massimo Mangino, Pim van der Harst, et al.Nature Genetics|July 1, 1997
Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in DrosophilaB Cohen, A Bashirullah, L Dagnino, et al.Nature Genetics|July 1, 1997
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va geneE Pastural, F J Barrat, R Dufourcq-Lagelouse, et al.Nature Genetics|July 1, 1997
Partial rescue of Brca1 (5-6) early embryonic lethality by p53 or p21 null mutationR Hakem, J L de la Pompa, A Elia, et al.Nature Genetics|July 1, 1997
Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 geneR S Jackson, J W Creemers, S Ohagi, et al.Nature Genetics|August 1, 1997
Functional genomics in mice by tagged sequence mutagenesisG G Hicks, E G Shi, X M Li, et al.Pageof 745