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Stella, G
Selicorni, A
Camera, G
Citation: F. Faravelli et al., Brachyphalangy, feet polydactyly, absent/hypoplastic tibiae: a further case and review of main diagnostic findings, CLIN DYSMOR, 10(2), 2001, pp. 101-103
Authors:
Bonglia, MC
Giorda, R
Borgatti, R
Felisari, G
Gagliardi, C
Selicorni, A
Zuffardi, O
Citation: Mc. Bonglia et al., Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome, AM J HU GEN, 69(2), 2001, pp. 261-268
Authors:
Ferrante, MI
Giorgio, G
Feather, SA
Bulfone, A
Wright, V
Ghiani, M
Selicorni, A
Gammaro, L
Scolari, F
Woolf, AS
Sylvie, O
Bernard, LM
Malcolm, S
Winter, R
Ballabio, A
Franco, B
Citation: Mi. Ferrante et al., Identification of the gene for oral-facial-digital type I syndrome, AM J HU GEN, 68(3), 2001, pp. 569-576
Authors:
Russo, S
Bedeschi, MF
Cogliati, F
Natacci, F
Gianotti, A
Parini, R
Selicorni, A
Larizza, L
Citation: S. Russo et al., Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1biallelic expression, CLIN DYSMOR, 9(3), 2000, pp. 157-162
Citation: A. Selicorni et F. Faravelli, Malpuech syndrome: A possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotype, AM J MED G, 95(3), 2000, pp. 291-291
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