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European Journal of Human Genetics : EJHG|November 26, 1999
Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2M Genuardi, S Carrara, M Anti, et al.European Journal of Human Genetics : EJHG|September 26, 2001
Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastomaM Genuardi, M Klutz, K Devriendt, et al.Journal of Medical Genetics|October 1, 1993
Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3L Kozák, P Chiurazzi, M Genuardi, et al.Cancer Detection and Prevention|January 1, 1991
Genomic changes on the short arm of human chromosome 1 in breast cancerW M Mars, M Genuardi, H Tsihira, et al.Cancer Genetics and Cytogenetics|July 15, 1988
Long-term cytogenetic effects of antineoplastic treatment in relation to secondary leukemiaM Genuardi, M Zollino, A Serra, et al.American Journal of Medical Genetics|May 1, 1994
Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European familiesU Orth, F Gurrieri, A Behmel, et al.American Journal of Medical Genetics|July 12, 1996
Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan populationP Chiurazzi, G Destro-Bisol, M Genuardi, et al.Leukemia Research|January 1, 1991
Chronic myelogenous leukemia in the course of chronic lymphocytic leukemia: evidence for an independent clonal originM Zollino, M Genuardi, P Tanci, et al.Genes, Chromosomes & Cancer|July 4, 2001
CDKN2A germline splicing mutation affecting both p16(ink4) and p14(arf) RNA processing in a melanoma/neurofibroma kindredF Petronzelli, D Sollima, G Coppola, et al.Human Mutation|June 1, 2001
Four novel MSH2 and MLH1 frameshift mutations and occurrence of a breast cancer phenocopy in hereditary nonpolyposis colorectal cancerO Caluseriu, E L Cordisco, A Viel, et al.Pageof 9