A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome

著者: Palumbo, O., Mattina, T., Palumbo, P., Carella, M., Perrotta, C.S.
出版事項 2014

Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

著者: Donaudy, F, Zheng, L, Ficarella, R, Ballana, E, Carella, M, Melchionda, S, Estivill, X, Bartles, J R, Gasparini, P
出版事項 2006

MicroRNA expression profiling in male and female familial breast cancer

著者: Pinto, R, De Summa, S, Danza, K, Popescu, O, Paradiso, A, Micale, L, Merla, G, Palumbo, O, Carella, M, Tommasi, S
出版年 Br J Cancer (2014)

On the statistical assessment of classifiers using DNA microarray data

著者: Carella M, Liuni S, Savino M, Cotugno R, D'Addabbo A, Piepoli A, Maglietta R, Ancona N, Pesole G, Perri F
出版事項 2006-08-01

On the statistical assessment of classifiers using DNA microarray data

著者: Ancona, N, Maglietta, R, Piepoli, A, D'Addabbo, A, Cotugno, R, Savino, M, Liuni, S, Carella, M, Pesole, G, Perri, F
出版事項 2006

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

著者: Carella, M, Stewart, G, Ajetunmobi, J F, Perrotta, S, Grootenboer, S, Tchernia, G, Delaunay, J, Totaro, A, Zelante, L, Gasparini, P, Iolascon, A
出版事項 1998

22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review

著者: Garavelli, L., Rosato, S., Wischmeijer, A., Gelmini, C., Esposito, A., Mazzanti, L., Franchi, F., De Crescenzo, A., Palumbo, O., Carella, M., Riccio, A.
出版事項 2011

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.

著者: Carella, M, D'Ambrosio, L, Totaro, A, Grifa, A, Valentino, M A, Piperno, A, Girelli, D, Roetto, A, Franco, B, Gasparini, P, Camaschella, C
出版事項 1997

Juvenile hemochromatosis locus maps to chromosome 1q.

著者: Roetto, A, Totaro, A, Cazzola, M, Cicilano, M, Bosio, S, D'Ascola, G, Carella, M, Zelante, L, Kelly, A L, Cox, T M, Gasparini, P, Camaschella, C
出版事項 1999

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

著者: Molin, A-M, Andrieux, J, Koolen, D A, Malan, V, Carella, M, Colleaux, L, Cormier-Daire, V, David, A, de Leeuw, N, Delobel, B, Duban-Bedu, B, Fischetto, R, Flinter, F, Kjaergaard, S, Kok, F, Krepischi, A C, Le Caignec, C, Ogilvie, C Mackie, Maia, S, Mathieu-Dramard, M, Munnich, A, Palumbo, O, Papadia, F, Pfundt, R, Reardon, W, Receveur, A, Rio, M, Ronsbro Darling, L, Rosenberg, C, Sá, J, Vallee, L, Vincent-Delorme, C, Zelante, L, Bondeson, M-L, Annerén, G
出版事項 2011