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Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1996
Microsatellite instability in IVS3 of murine c-fes gene: tumor-associated rearrangement and mammalian divergenceL Volpi, A Beghini, D Rossi, et al.Molecular and Cellular Probes|June 17, 1999
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STRL Corrado, P Colapietro, L Larizza, et al.Hematological Oncology|July 1, 1995
Identification of chromosomal rearrangements in the human myeloid leukemia cell line GF-D8 by dual-colour fluorescence in situ hybridizationL Doneda, A Biondi, A Rambaldi, et al.Cancer Genetics and Cytogenetics|August 1, 1987
Mosaicism in the C-banded region of chromosome 1 in cancer familiesL Doneda, A F Conti, V Gualandri, et al.Annales De Genetique|January 1, 1993
Prenatal diagnosis of an extranumerary i(22p) with normal phenotypeL Doneda, L Dalprà, M G Tibiletti, et al.Cytotechnology|February 24, 2012
Localization of viral transforming sequences within marker chromosomes associated with tumor formation and progression in a murine fibrosarcomaL Doneda, P Custode, C de G Morghen, et al.Cancer Genetics and Cytogenetics|July 1, 1991
Karyotypic characterization of a new human embryonal rhabdomyosarcoma cell lineI Magnani, F Faustinella, P Nanni, et al.Annals of Human Genetics|September 6, 2005
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion intervalM Venturin, A Bentivegna, R Moroni, et al.Journal of the National Cancer Institute|June 1, 1984
Inheritance of immunogenicity and metastatic potential in murine cell hybrids from the T-lymphoma ESb08 and normal spleen lymphocytesL Larizza, V Schirrmacher, M Stöhr, et al.American Journal of Medical Genetics|March 3, 1997
Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndromeP Castorina, A Selicorni, F Bedeschi, et al.Pageof 11