FRACCARO, MARCO

FRACCARO, MARCO  

DIPARTIMENTO DI PATOLOGIA UMANA ED EREDITARIA (attivo dal 01/01/1900 al 28/02/2011)  

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Titolo Data di pubblicazione Autore(i) File
"Cri du chat" syndrome due to a complex rearrangement of chromosome 5 1-gen-1978 Francesconi, D; Zuffardi, Orsetta; D'Attoma, G; Fraccaro, Marco
15/15 translocation in Prader-Willi syndrome. 1-gen-1977 Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Jurik, Lp
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease. 1-gen-1989 Scappaticci, MARIA ASSUNTA; Lambaise, S; Fraccaro, Marco; Orecchia, Giovanni
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease 1-gen-1989 Scappaticci, MARIA ASSUNTA; Lambiase, Simonetta; Fraccaro, Marco; Orecchia, Giovanni
A deletion of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis 1-gen-1991 Bardoni, B; Zuffardi, Orsetta; Guioli, S; Ballabio, A; Simi, P; Cavalli, P; Grimoldi, Mg; Fraccaro, Marco; Camerino, G.
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal 1-gen-1994 Bardoni, B; Zanaria, E; Floridia, G; Worley, Kc; Toini, G; Ferrante, E; Chiumello, G; Mccabe, Erb; Fraccaro, Marco; Zuffardi, Orsetta; Camerino, G.
A novel mechnaism for the origin of supernumerary marker chromosomes 1-gen-1996 Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco
Antenatal sex detrmination 1-gen-1984 Simoni, G; Brambati, B; Danesino, Cesare; Fraccaro, Marco
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. 1-gen-1980 Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Di Natale, B; Gargantini, L; Muller, Cr; Ropers, Hh
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities. 1-gen-1978 Kinross, J; Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Tiepolo, Luciano; Zuffardi, Orsetta; Pawlowitzki, Ih; Jones, Kw
Chromosome 15 and Prader-Willi syndrome 1-gen-1978 Zuffardi, Orsetta; Buhler, Em; Fraccaro, Marco
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology 1-gen-1981 Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Giarola, A.
Chromosome abnormalities in Dyskeratosis congenita. 1-gen-1989 Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D.
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. 1-gen-1991 Scappaticci, MARIA ASSUNTA; Maraschio, Paola; del Ciotto, N; Fossati, Gs; Zonta, Aris; Fraccaro, Marco
Chromosome abnormalities in Tuberous Sclerosis. 1-gen-1988 Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M; Vivarelli R., Fois A; Fraccaro, Marco
Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41). 1-gen-1974 Fraccaro, Marco; LO CURTO, Francesco; Scappaticci, MARIA ASSUNTA
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125). 1-gen-1972 Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Fraccaro, Marco
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli. 1-gen-1989 Scappaticci, MARIA ASSUNTA; Lambiase, Simonetta; Orecchia, Giovanni; Fraccaro, Marco
Clonal structural chromosomal rearrangements in primary fibroblastic cultures and in lymphocytes of patients with Werner's syndroe. 1-gen-1982 Scappaticci, MARIA ASSUNTA; Cerimele, D; Fraccaro, Marco
Correlation between testicular tissue and H-Y phenotype in intersex patients 1-gen-1983 Muller, U; Mayerova, A; Debus, B; Fraccaro, Marco; Gilgenkrants, S; Glatzl, J; Madan, K; Pfeiffer, Ra; Prader, A; Zuffardi, Orsetta