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Oncogene|October 14, 2000
Identification and characterization of JunD missense mutants that lack menin bindingJ I Knapp, C Heppner, A B Hickman, et al.Oncogene|November 11, 1999
Stable overexpression of MEN1 suppresses tumorigenicity of RASY S Kim, A L Burns, P K Goldsmith, et al.Cell|November 15, 1996
Failure of embryonic hematopoiesis and lethal hemorrhages in mouse embryos heterozygous for a knocked-in leukemia gene CBFB-MYH11L H Castilla, C Wijmenga, Q Wang, et al.American Journal of Human Genetics|October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21D E Merry, J G Lesko, D M Sosnoski, et al.American Journal of Human Genetics|February 1, 1991
Two frameshift mutations in the cystic fibrosis geneM C Iannuzzi, R C Stern, F S Collins, et al.Human Heredity|June 12, 1999
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigatorsR M Watanabe, T Valle, E R Hauser, et al.Journal of the National Cancer Institute. Monographs|January 1, 1995
Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutationsF J Couch, J Garber, S Kiousis, et al.Biotechniques|October 1, 1996
Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: implications for PCR-based genotyping and cloningV L Magnuson, D S Ally, S J Nylund, et al.Genomics|September 1, 1993
Multicolor FISH mapping with Alu-PCR-amplified YAC clone DNA determines the order of markers in the BRCA1 region on chromosome 17q12-q21W L Flejter, C L Barcroft, S W Guo, et al.Genomics|December 1, 1991
cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene productD A Marchuk, A M Saulino, R Tavakkol, et al.Pageof 24