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Results:
1-12
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Results: 12
Authors:
Nicolao, P
Carella, M
Giometto, B
Tavolato, B
Cattin, R
Giovannucci-Uzielli, ML
Vacca, M
Della Regione, F
Piva, S
Bortoluzzi, S
Gasparini, P
Citation: P. Nicolao et al., DHPLC analysis of the MECP2 gene in Italian Rett patients, HUM MUTAT, 18(2), 2001, pp. 132-140
Authors:
Carella, AM
Beltrami, G
Carella, M
Corsetti, MT
Scalzulli, RP
Greco, M
Citation: Am. Carella et al., Immunosuppressive non-myeloablative allografting as salvage therapy in advanced Hodgkin's disease, HAEMATOLOG, 86(11), 2001, pp. 1121-1123
Authors:
Carella, M
Pace, R
Citation: M. Carella et R. Pace, Some migration dynamics specific to southern Europe: South-north and east-west axis, INT MIGR, 39(4), 2001, pp. 63-99
Authors:
Melchionda, S
Ahituv, N
Bisceglia, L
Sobe, T
Glaser, F
Rabionet, R
Arbones, ML
Notarangelo, A
Di Iorio, E
Carella, M
Zelante, L
Estivill, X
Avraham, KB
Gasparini, P
Citation: S. Melchionda et al., MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss, AM J HU GEN, 69(3), 2001, pp. 635-640
Authors:
Pointon, JJ
Merryweather-Clarke, AT
Carella, M
Robson, KJH
Citation: Jj. Pointon et al., Detection of C282Y and H63D in the HFE gene, GENET TEST, 4(2), 2000, pp. 115-120
Authors:
Camaschella, C
Roetto, A
Cali, A
De Gobbi, M
Garozzo, G
Carella, M
Majorano, N
Totaro, A
Gasparini, P
Citation: C. Camaschella et al., The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22, NAT GENET, 25(1), 2000, pp. 14-15
Authors:
Carella, M
Fulignati, P
Musumeci, G
Sbrana, A
Citation: M. Carella et al., Metamorphic consequences of Neogene thermal anomaly in the northern Apennines (Radicondoli-Travale area, Larderello geothermal field Italy), GEODIN ACTA, 13(6), 2000, pp. 345-366
Authors:
Iolascon, A
Servedio, V
Carbone, R
Totaro, A
Carella, M
Perrotta, S
Wickramasinghe, SN
Delaunay, J
Heimpel, H
Gasparini, P
Citation: A. Iolascon et al., Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?, HAEMATOLOG, 85(5), 2000, pp. 470-474
Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome
Authors:
Seri, M
Melchionda, S
Dreyer, S
Marini, M
Carella, M
Cusano, R
Piemontese, MR
Caroli, F
Silengo, M
Zelante, L
Romeo, G
Ravazzolo, R
Gasparini, P
Lee, B
Citation: M. Seri et al., Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome, INT J MOL M, 4(3), 1999, pp. 285-290
Authors:
Carella, M
Stewart, GW
Ajetunmobi, JF
Schettini, F
Delaunay, J
Iolascon, A
Citation: M. Carella et al., Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia, HAEMATOLOG, 84(9), 1999, pp. 862-863
Authors:
Iolascon, A
Stewart, GW
Ajetunmobi, JF
Perrotta, S
Delaunay, J
Carella, M
Zelante, L
Gasparini, P
Citation: A. Iolascon et al., Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis), BLOOD, 93(9), 1999, pp. 3120-3123
Authors:
Roetto, A
Totaro, A
Cazzola, M
Cicilano, M
Bosio, S
D'Ascola, G
Carella, M
Zelante, L
Kelly, AL
Cox, TM
Gasparini, P
Camaschella, C
Citation: A. Roetto et al., Juvenile hemochromatosis locus maps to chromosome 1q, AM J HU GEN, 64(5), 1999, pp. 1388-1393
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