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Results:
1-20
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Results: 20
Authors:
Tonini, GP
McConville, C
Cusano, R
Rees, SA
Dagnino, M
Longo, L
De Bernardi, B
Conte, M
Garaventa, A
Romeo, G
Devoto, M
Seri, M
Citation: Gp. Tonini et al., Exclusion of candidate genes and chromosomal regions in familial neuroblastoma, INT J MOL M, 7(1), 2001, pp. 85-89
Authors:
Devoto, M
Specchia, C
Li, HH
Caminis, J
Tenenhouse, A
Rodriguez, H
Spotila, LD
Citation: M. Devoto et al., Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36, HUM MOL GEN, 10(21), 2001, pp. 2447-2452
Authors:
Shugart, YY
Specchia, C
Li, HH
Doan, BQ
Mathias, RA
Devoto, M
Citation: Yy. Shugart et al., Comparison of sib pair-based approaches for identifying quantitative traitloci underlying asthma in the Busselton families, GENET EPID, 21, 2001, pp. S198-S203
Authors:
Iolascon, A
Giordano, P
Storelli, S
Li, HH
Coppola, B
Piga, A
Fantola, E
Forni, G
Cianciulli, P
Perrotta, S
Magnano, C
Maggio, A
Mangiagli, A
Devoto, M
Citation: A. Iolascon et al., Thrombophilia in thalassemia major patients: analysis of genetic predisposing factors, HAEMATOLOG, 86(10), 2001, pp. 1112-1113
Authors:
Vitale, E
Specchia, C
Devoto, M
Angius, A
Rong, S
Rocchi, M
Schwalb, M
Demelas, L
Paglietti, D
Manca, S
Mastropaolo, C
Serra, G
Citation: E. Vitale et al., Novel X-linked mental retardation syndrome with short stature maps to Xq24, AM J MED G, 103(1), 2001, pp. 1-8
Authors:
Krantz, ID
Tonkin, E
Smith, M
Devoto, M
Bottani, A
Simpson, C
Hofreiter, M
Abraham, V
Jukofsky, L
Conti, BP
Strachan, T
Jackson, L
Citation: Id. Krantz et al., Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange Syndrome, AM J MED G, 101(2), 2001, pp. 120-129
Authors:
Vitale, E
Brancolini, V
De Rienzo, A
Bird, L
Allada, V
Sklansky, M
Chae, CU
Ferrero, G
Weber, J
Devoto, M
Casey, B
Citation: E. Vitale et al., Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p, J MED GENET, 38(3), 2001, pp. 182-185
Authors:
Bolino, A
Muglia, M
Conforti, FL
LeGuern, E
Salih, MAM
Georgiou, DM
Christodoulou, K
Hausmanowa-Petrusewicz, I
Mandich, P
Schenone, A
Gambardella, A
Bono, F
Quattrone, A
Devoto, M
Monaco, AP
Citation: A. Bolino et al., Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2, NAT GENET, 25(1), 2000, pp. 17-19
Authors:
Griseri, P
Sancandi, M
Patrone, G
Bocciardi, R
Hofstra, R
Ravazzolo, R
Devoto, M
Romeo, G
Ceccherini, I
Citation: P. Griseri et al., A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease, EUR J HUM G, 8(9), 2000, pp. 721-724
Authors:
Forabosco, P
Collins, A
Latiano, A
Annese, V
Clementi, M
Andriulli, A
Fortina, P
Devoto, M
Morton, NE
Citation: P. Forabosco et al., Combined segregation and linkage analysis of inflammatory bowel disease inthe IBD1 region using severity to characterise Crohn's disease and ulcerative colitis, EUR J HUM G, 8(11), 2000, pp. 846-852
Authors:
Lo Nigro, C
Cusano, R
Scaranari, M
Cinti, R
Forabosco, P
Morra, VB
De Michele, G
Santoro, L
Davies, S
Hurst, J
Devoto, M
Ravazzolo, R
Seri, M
Citation: C. Lo Nigro et al., A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2, EUR J HUM G, 8(10), 2000, pp. 777-782
Authors:
Bolino, A
Levy, ER
Muglia, M
Conforti, FL
LeGuern, E
Salih, MAM
Georgiou, DM
Hausmanowa-Petrusewicz, I
Mandich, P
Gambardella, A
Quattrone, A
Devoto, M
Monaco, AP
Citation: A. Bolino et al., Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22, GENOMICS, 63(2), 2000, pp. 271-278
Authors:
del Giudice, EM
Perrone, L
Forabosco, P
Devoto, M
Carbone, MT
Calabro, C
Di Toro, R
Citation: Em. Del Giudice et al., Linkage study of early-onset obesity to leptin receptor gene in Italian children, NUTR RES, 20(8), 2000, pp. 1059-1063
Authors:
Annese, V
Latiano, A
Bovio, P
Forabosco, P
Piepoli, A
Lombardi, G
Andreoli, A
Astegiano, M
Gionchetti, P
Riegler, G
Sturniolo, GC
Clementi, M
Rappaport, E
Fortina, P
Devoto, M
Gasparini, P
Andriulli, A
Citation: V. Annese et al., Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus - A GISC study, EUR J HUM G, 7(5), 1999, pp. 567-573
Authors:
Golnik, KC
Devoto, M
Kersten, RC
Kulwin, D
Citation: Kc. Golnik et al., Visual loss in idiopathic intracranial hypertension after resolution of papilledema, OPHTHAL PL, 15(6), 1999, pp. 442-444
Authors:
Fimiani, M
Seri, M
Rubegni, P
Cusano, R
De Aloe, G
Forabosco, P
Devoto, M
Andreassi, L
Renieri, A
Citation: M. Fimiani et al., Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regions, ARCH DERM R, 291(12), 1999, pp. 637-642
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
Authors:
Andrew, LJ
Brancolini, V
de la Pena, LS
Devoto, M
Caeiro, F
Marchegiani, R
Reginato, A
Gaucher, A
Netter, P
Gillet, P
Loeuille, D
Prockop, DJ
Carr, A
Wordsworth, BF
Lathrop, M
Butcher, S
Considine, E
Everts, K
Nicod, A
Walsh, S
Williams, CJ
Citation: Lj. Andrew et al., Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease, AM J HU GEN, 64(1), 1999, pp. 136-145
Authors:
Bolino, A
Seri, M
Caroli, F
Eubanks, J
Srinivasan, J
Mandich, P
Schenone, A
Quattrone, A
Romeo, G
Catterall, WA
Devoto, M
Citation: A. Bolino et al., Exclusion of the SCN2B gene as candidate for CMT4B, EUR J HUM G, 6(6), 1998, pp. 629-634
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
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