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Results: 1-10 |
Results: 10
Genotype-phenotype correlations in Wolf-Hirschhoun syndrome
Authors: Zollino, M Neri, G
Citation: M. Zollino et G. Neri, Genotype-phenotype correlations in Wolf-Hirschhoun syndrome, EUR J HUM G, 9(2), 2001, pp. 150-150
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations
Authors: Rossi, E Piccini, F Zollino, M Neri, G Caselli, D Tenconi, R Castellan, C Carrozzo, R Danesino, C Zuffardi, O Ragusa, A Castiglia, L Galesi, O Greco, D Romano, C Pierluigi, M Perfumo, C Di Rocco, M Faravelli, F Bricarelli, FD Bonaglia, M Bedeschi, M Borgatti, R
Citation: E. Rossi et al., Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations, J MED GENET, 38(6), 2001, pp. 417-420
The association of severe aplastic anaemia with the Philadelphia chromosome and the BCR/ABL transcript
Authors: Sica, S Chiusolo, P Zollino, M Sora, F Piccirillo, N Laurenti, L Reddiconto, G Leone, G
Citation: S. Sica et al., The association of severe aplastic anaemia with the Philadelphia chromosome and the BCR/ABL transcript, BR J HAEM, 114(4), 2001, pp. 961-962
Secondary myelodysplastic syndromes following peripheral blood stem cell transplantation: morphological, cytogenetic and clonality evaluation and thelimitation of FAB criteria
Authors: Laurenti, L d'Onofrio, G Sica, S Chiusolo, P Zini, G Piccirillo, N Zollino, M Garzia, M Sora', F Leone, G
Citation: L. Laurenti et al., Secondary myelodysplastic syndromes following peripheral blood stem cell transplantation: morphological, cytogenetic and clonality evaluation and thelimitation of FAB criteria, BONE MAR TR, 26(2), 2000, pp. 241-242
Partial deletion of chromosome 12q is not usually associated with CFC syndrome
Authors: Zollino, M Neri, G
Citation: M. Zollino et G. Neri, Partial deletion of chromosome 12q is not usually associated with CFC syndrome, AM J MED G, 95(3), 2000, pp. 296-296
Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome
Authors: Zollino, M Di Stefano, C Zampino, G Mastroiacovo, P Wright, TJ Sorge, G Selicorni, A Tenconi, R Zappala, A Battaglia, A Di Rocco, M Palka, G Pallotta, R Altherr, MR Neri, G
Citation: M. Zollino et al., Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome, AM J MED G, 94(3), 2000, pp. 254-261
Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: A pitfall in prenatal diagnosis
Authors: Zollino, M Bajer, J Neri, G
Citation: M. Zollino et al., Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: A pitfall in prenatal diagnosis, PRENAT DIAG, 19(2), 1999, pp. 184-185
Partial duplication of the long arm of chromosome 15: Confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome
Authors: Zollino, M Tiziano, F Di Stefano, C Neri, G
Citation: M. Zollino et al., Partial duplication of the long arm of chromosome 15: Confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome, AM J MED G, 87(5), 1999, pp. 391-394
"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype
Authors: Zollino, M Wright, TJ Di Stefano, C Tosolini, A Battaglia, A Altherr, MR Neri, G
Citation: M. Zollino et al., "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype, AM J MED G, 82(5), 1999, pp. 371-375
Association of trisomy 9p and band heterotopia
Authors: Federico, A Tomasetti, P Zollino, M Diomedi, M Dotti, MT De Stefano, N Gualdi, GF Neri, G Gigli, GL
Citation: A. Federico et al., Association of trisomy 9p and band heterotopia, NEUROLOGY, 53(2), 1999, pp. 430-432
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