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Human Genetics|January 1, 1982
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's SyndromeS Scappaticci, D Cerimele, M FraccaroHuman Genetics|December 23, 1977
Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertileM Fraccaro, P Maraschio, F Pasquali, et al.Pediatric Dermatology|March 1, 1994
Treatment of severe alopecia areata with squaric acid dibutylester in pediatric patientsG Orecchia, P Malagoli, L SantagostinoMonaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|November 26, 2003
A case of indirect exposure to cat at schoolM Ferrari, L Perfetti, G MoscatoMonaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|March 25, 1998
Clinical evaluation of occupational asthmaG Moscato, L Perfetti, E GaldiAnnales De Genetique|September 1, 1977
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromereP Maraschio, S Scappaticci, E Ferrari, et al.Journal of Endocrinological Investigation|July 6, 2004
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children?C Olivieri, C Danesino, S Scappaticci, et al.Acta Dermato-Venereologica|January 1, 1979
Chronic bullous dermatosis of childhoodC Del Forno, A Giannetti, G OrecchiaCancer 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|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.Pageof 11