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Results: 51-66/66
Authors:
Digilio, MC
Marino, B
Toscano, A
Giannotti, A
Dallapiccola, B
Citation: Mc. Digilio et al., Atrioventricular canal defect without Down syndrome: A heterogeneous malformation, AM J MED G, 85(2), 1999, pp. 140-146
Authors:
Digilio, MC
Marino, B
Bevilacqua, M
Musolino, AM
Giannotti, A
Dallapiccola, B
Citation: Mc. Digilio et al., Genetic heterogeneity of isolated noncompaction of the left ventricular myocardium, AM J MED G, 85(1), 1999, pp. 90-91
Authors:
Digilio, MC
Marino, B
Ammirati, A
Borzaga, U
Giannotti, A
Dallapiccola, B
Citation: Mc. Digilio et al., Cardiac malformations in patients with oral-facial-skeletal syndromes: Clinical similarities with heterotaxia, AM J MED G, 84(4), 1999, pp. 350-356
Authors:
Digilio, MC
Marino, B
Giannico, S
Giannotti, A
Dallapiccola, B
Citation: Mc. Digilio et al., Atrioventricular canal defect and hypoplastic left heart syndrome as discordant congenital heart defects in twins, TERATOLOGY, 60(4), 1999, pp. 206-208
Authors:
Servidei, S
Capon, F
Spinazzola, A
Mirabella, M
Semprini, S
de Rosa, G
Gennarelli, M
Sangiuolo, F
Ricci, E
Mohrenweiser, HW
Dallapiccola, B
Tonali, P
Novelli, G
Citation: S. Servidei et al., A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13, NEUROLOGY, 53(4), 1999, pp. 830-837
Authors:
Marino, B
Digilio, MC
Toscano, A
Giannotti, A
Dallapiccola, B
Citation: B. Marino et al., Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal, J PEDIAT, 135(6), 1999, pp. 703-706
Authors:
Botta, A
Novelli, G
Mari, A
Novelli, A
Sabani, M
Korenberg, J
Osborne, LR
Digilio, MC
Giannotti, A
Dallapiccola, B
Citation: A. Botta et al., Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes, J MED GENET, 36(6), 1999, pp. 478-480
Authors:
Digilio, MC
Marino, B
Bagolan, P
Giannotti, A
Dallapiccola, B
Citation: Mc. Digilio et al., Microdeletion 22q11 and oesophageal atresia, J MED GENET, 36(2), 1999, pp. 137-139
Authors:
Capon, F
Novelli, G
Semprini, S
Clementi, M
Nudo, M
Vultaggio, P
Mazzanti, C
Gobello, T
Botta, A
Fabrizi, G
Dallapiccola, B
Citation: F. Capon et al., Searching for psoriasis susceptibility genes in Italy: Genome scan and evidence for a new locus on chromosome 1, J INVES DER, 112(1), 1999, pp. 32-35
Authors:
Schiaffino, S
Dallapiccola, B
Di Lisi, R
Citation: S. Schiaffino et al., Molecular genetics of congenital heart disease - A problem of faulty septation, CIRCUL RES, 84(2), 1999, pp. 247-249
Authors:
Colosimo, A
Serafino, A
Sangiuolo, F
Di Sario, S
Bruscia, E
Amicucci, P
Novelli, G
Dallapiccola, B
Mossa, G
Citation: A. Colosimo et al., Gene transfection efficiency of tracheal epithelial cells by DC-Chol-DOPE/DNA complexes, BBA-BIOMEMB, 1419(2), 1999, pp. 186-194
Authors:
Capon, F
Semprini, S
Dallapiccola, B
Novelli, G
Citation: F. Capon et al., Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21, AM J HU GEN, 65(6), 1999, pp. 1798-1800
Authors:
Mangino, M
Sanchez, O
Torrente, I
De Luca, A
Capon, F
Novelli, G
Dallapiccola, B
Citation: M. Mangino et al., Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22, AM J HU GEN, 65(2), 1999, pp. 441-447
Authors:
Wadey, R
McKie, J
Papapetrou, C
Sutherland, H
Lohman, F
Osinga, J
Frohn, I
Hofstra, R
Meijers, C
Amati, F
Conti, E
Pizzuti, A
Dallapiccola, B
Novelli, G
Scambler, P
Citation: R. Wadey et al., Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11, AM J HU GEN, 65(1), 1999, pp. 247-249
Authors:
Marino, B
Digilio, MC
Persiani, M
Di Donto, R
Toscano, A
Giannotti, A
Dallapiccola, B
Citation: B. Marino et al., Deletion 22q11 in patients with interrupted aortic arch, AM J CARD, 84(3), 1999, pp. 360
Authors:
De Luca, A
Torrente, I
Mangino, M
Bertini, E
Dallapiccola, B
Novelli, G
Citation: A. De Luca et al., A novel mutation (R27 1X) in the myotubularin gene causes a severe miotubular myopathy, HUMAN HERED, 49(1), 1999, pp. 59-60