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The New England Journal of Medicine|April 3, 1986
Trisomy 12 in B cells of patients with B-cell chronic lymphocytic leukemiaS Knuutila, E Elonen, L Teerenhovi, et al.Oncogene|July 23, 1998
Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instabilityA Percesepe, P Kristo, L A Aaltonen, et al.Blood|September 25, 1999
Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous stateS S Watowich, X Xie, U Klingmuller, et al.Genes, Chromosomes & Cancer|October 27, 1999
Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindredsM Nyström-Lahti, M Holmberg, P Fidalgo, et al.Cancer Research|August 17, 2002
Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangementsHidewaki Nakagawa, Hai Yan, Janet Lockman, et al.Scandinavian Journal of Haematology|August 1, 1981
The 5q- chromosome in preleukaemia and acute leukaemiaL Teerenhovi, G H Borgström, R Lintula, et al.Proceedings of the National Academy of Sciences of the United States of America|January 24, 2009
Polymorphic mature microRNAs from passenger strand of pre-miR-146a contribute to thyroid cancerKrystian Jazdzewski, Sandya Liyanarachchi, Michal Swierniak, et al.The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor geneK Aittomäki, R Herva, U H Stenman, et al.Human Genetics|January 1, 1980
H-Y antigen in 46,XY gonadal dysgenesisS S Wachtel, G C Koo, A de la Chapelle, et al.Pageof 61