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Results: 1-5 |
Results: 5

Authors: Clauser, L Galie, M Hassanipour, A Calabrese, O
Citation: L. Clauser et al., Saethre-Chotzen syndrome: Review of the literature and report of a case, J CRANIOF S, 11(5), 2000, pp. 480-486

Authors: Sensi, A Gualandi, F Pittalis, MC Calabrese, O Falciano, F Maestri, I Bovicelli, L Calzolari, E
Citation: A. Sensi et al., Mole maker phenotype: possible narrowing of the candidate region, EUR J HUM G, 8(8), 2000, pp. 641-644

Authors: Filla, A Mariotti, C Caruso, G Coppola, G Cocozza, S Castaldo, I Calabrese, O Salvatore, E De Michele, G Riggio, MC Pareyson, D Gellera, C Di Donato, S
Citation: A. Filla et al., Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families, EUR NEUROL, 44(1), 2000, pp. 31-36

Authors: Filla, A De Michele, G Santoro, L Calabrese, O Castaldo, I Giuffrida, S Restivo, D Serlenga, L Condorelli, DF Bonuccelli, U Scala, R Coppola, G Caruso, G Cocozza, S
Citation: A. Filla et al., Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families, J NEUROL, 246(6), 1999, pp. 467-471

Authors: Gualandi, F Sensi, A Calabrese, O Gruppioni, R Pittalis, MC Calzolari, E
Citation: F. Gualandi et al., Prenatal exclusion of UPD from cytogenetic slides: A simple method, PRENAT DIAG, 19(1), 1999, pp. 87-88
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