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Results:
1-7
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Results: 7
Authors:
Wazlawick, RS
Rosatelli, MC
Ramos, EMF
Cybis, WA
Storb, BH
Schuhmacher, VRN
Mariani, AC
Kirner, T
Kirner, C
Fagundes, LC
Citation: Rs. Wazlawick et al., Providing more interactivity to virtual museums: A proposal for a VR authoring tool, PRESENCE-T, 10(6), 2001, pp. 647-656
Authors:
Saxena, R
Moi, L
Demurtas, M
Rosatelli, MC
Cao, A
Verma, IC
Citation: R. Saxena et al., A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACTCCT GAG ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing, I J MED RES, 111, 2000, pp. 24-27
Authors:
Miralles, IM
Montana, AV
Rosatelli, MC
Mameli, C
Gilabert, PB
Citation: Im. Miralles et al., Thalassemic trait caused by IVSII-1 (G -> A) mutation detected in a Spanish family, HAEMATOLOG, 85(11), 2000, pp. 1215-1216
Authors:
Perniola, R
Magliari, F
Rosatelli, MC
De Marzi, CA
Citation: R. Perniola et al., High-risk pregnancy in beta-thalassemia major women - Report of three cases, GYNECOL OBS, 49(2), 2000, pp. 137-139
Authors:
Iolascon, A
Meloni, A
Coppola, B
Rosatelli, MC
Citation: A. Iolascon et al., Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5 '-diphosphate-glucuronosyltransferase (UGT1A1) gene, J MED GENET, 37(9), 2000, pp. 712-713
Authors:
Cao, A
Galanello, R
Rosatelli, MC
Citation: A. Cao et al., Prenatal diagnosis and screening of the haemoglobinopathies, BAIL CLIN H, 11(1), 1998, pp. 215-238
Authors:
Rosatelli, MC
Meloni, A
Meloni, A
Devoto, M
Cao, A
Scott, HS
Peterson, P
Heino, M
Krohn, KJE
Nagamine, K
Kudoh, J
Shimizu, N
Antonarakis, SE
Citation: Mc. Rosatelli et al., A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients, HUM GENET, 103(4), 1998, pp. 428-434
Risultati:
1-7
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