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Cancer Genetics and Cytogenetics|March 1, 1992
Cytogenetics of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasiaS Scappaticci, G Arrigoni, E Capra, et al.Human Genetics|January 19, 1979
A homozygote for a serum albumin variant of the fast typeG Vanzetti, F Porta, L Prencipe, et al.Human Genetics|April 1, 1986
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcomaS Scappaticci, D Cerimele, F Cottoni, et al.Human Genetics|June 10, 1977
Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18V Vigi, P Maraschio, G Bosi, et al.Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, et al.Annales De Genetique|January 1, 1990
Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndromeS Scappaticci, A Forabosco, G Borroni, et al.Journal of Medical Genetics|August 1, 1977
15/15 translocation in Prader-Willi syndromeM Fraccaro, O Zuffardi, E M Buhler, et al.Cytogenetics and Cell Genetics|January 1, 1989
Analysis of complex Y chromosome aberrations using a single DNA probe (Y-367)U Müller, D Fontaine, M Adinolfi, et al.Human Genetics|May 1, 1992
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2R Avarello, A Pedicini, A Caiulo, et al.Cancer Genetics and Cytogenetics|February 15, 2001
Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator geneA Minelli, E Maserati, G Giudici, et al.Pageof 9