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Results:
1-15
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Results: 15
Authors:
Priolo, M
De Toni, T
Baffico, M
Cama, A
Seri, M
Cusano, R
Costabello, L
Fondelli, P
Capra, V
Silengo, M
Ravazzolo, R
Lerone, M
Citation: M. Priolo et al., Fontaine-Farriaux craniosynostosis: Second report in the literature, AM J MED G, 100(3), 2001, pp. 214-218
Authors:
Priolo, M
Rosaia, L
Seri, M
Silengo, MC
Ravazzolo, R
Lerone, M
Citation: M. Priolo et al., Total anonychia congenita in a woman with normal intelligence: Report of afurther case, DERMATOLOGY, 200(1), 2000, pp. 84-85
Authors:
Priolo, M
Lerone, M
Rosaia, L
Calcagno, EP
Sadeghi, AK
Ghezzi, F
Ravazzolo, R
Silengo, M
Citation: M. Priolo et al., Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?, CLIN DYSMOR, 9(4), 2000, pp. 277-280
Authors:
Silengo, M
Lerone, M
Seri, M
Priolo, M
Jarre, L
Citation: M. Silengo et al., New clinical findings in oculo-ectodermal syndrome, CLIN DYSMOR, 9(1), 2000, pp. 39-41
Authors:
De Biasio, P
Prefumo, F
Baffico, M
Baldi, M
Priolo, M
Lerone, M
Toma, P
Venturini, PL
Citation: P. De Biasio et al., Sonographic and molecular diagnosis of thanatophoric dysplasia type I at 18 weeks of gestation, PRENAT DIAG, 20(10), 2000, pp. 835-837
Authors:
Martucciello, G
Ceccherini, I
Lerone, M
Jasonni, V
Citation: G. Martucciello et al., Pathogenesis of Hirschsprung's disease, J PED SURG, 35(7), 2000, pp. 1017-1025
Authors:
Priolo, M
Silengo, M
Lerone, M
Ravazzolo, R
Citation: M. Priolo et al., Ectodermal dysplasias: not only 'skin' deep, CLIN GENET, 58(6), 2000, pp. 415-430
Authors:
Priolo, M
Lerone, M
Baffico, M
Baldi, M
Ravazzolo, R
Cama, A
Capra, V
Silengo, M
Citation: M. Priolo et al., Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene, CLIN GENET, 58(1), 2000, pp. 81-83
Authors:
Seri, M
Martucciello, G
Paleari, L
Bolino, A
Priolo, M
Salemi, G
Forabosco, P
Caroli, F
Cusano, R
Tocco, T
Lerone, M
Cama, A
Torre, M
Guys, JM
Romeo, G
Jasonni, V
Citation: M. Seri et al., Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndromeand anorectal malformations with sacral hypodevelopment, HUM GENET, 104(1), 1999, pp. 108-110
Authors:
Mori, PG
Priolo, M
Lerone, M
Caroli, F
Cusano, R
Seri, M
Silengo, MC
Citation: Pg. Mori et al., Congenital hypoplastic anaemia in a patient with a new multiple congenitalanomalies-mental retardation syndrome, AM J MED G, 87(1), 1999, pp. 36-39
Authors:
Bohring, A
Silengo, M
Lerone, M
Superneau, DW
Spaich, C
Braddock, SR
Poss, A
Opitz, JM
Citation: A. Bohring et al., Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?, AM J MED G, 85(5), 1999, pp. 438-446
Authors:
Basson, CT
Huang, TS
Lin, RC
Bachinsky, DR
Weremowicz, S
Vaglio, A
Bruzzone, R
Quadrelli, R
Lerone, M
Romeo, G
Silengo, M
Pereira, A
Krieger, J
Mesquita, SF
Kamisago, M
Morton, CC
Pierpont, MEM
Muller, CW
Seidman, JG
Seidman, CE
Citation: Ct. Basson et al., Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations, P NAS US, 96(6), 1999, pp. 2919-2924
Authors:
Silengo, M
Lerone, M
Seri, M
Boffi, P
Citation: M. Silengo et al., Reply to the letter by De Smet and Fryns. Symbrachydactyly involving both the hand and foot, CLIN GENET, 56(2), 1999, pp. 176-177
Authors:
Silengo, M
Lerone, M
Seri, M
Boffi, P
Citation: M. Silengo et al., Lower extremity counterpart of the Poland syndrome, CLIN GENET, 55(1), 1999, pp. 41-43
Authors:
Seri, M
Cusano, R
Forabosco, P
Cinti, R
Caroli, F
Picco, P
Bini, R
Morra, VB
De Michele, G
Lerone, M
Silengo, M
Pela, I
Borrone, C
Romeo, G
Devoto, M
Citation: M. Seri et al., Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy, AM J HU GEN, 64(2), 1999, pp. 586-593
Risultati:
1-15
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