Detection of aneuploidies by paralogous sequence quantification

Por Deutsch, S, Choudhury, U, Merla, G, Howald, C, Sylvan, A, Antonarakis, S
Publicado em 2004

Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel MLL2 Mutation

Por Ratbi, I., Fejjal, N., Micale, L., Augello, B., Fusco, C., Lyahyai, J., Merla, G., Sefiani, A.
Publicado em 2013

A 1.3-Mb 7q11.23 Atypical Deletion Identified in a Cohort of Patients with Williams-Beuren Syndrome

Por Delgado, L.M., Gutierrez, M., Augello, B., Fusco, C., Micale, L., Merla, G., Pastene, E.A.
Publicado em 2013

MicroRNA expression profiling in male and female familial breast cancer

Por Pinto, R, De Summa, S, Danza, K, Popescu, O, Paradiso, A, Micale, L, Merla, G, Palumbo, O, Carella, M, Tommasi, S
Publicado no Br J Cancer (2014)

Two high throughput technologies to detect segmental aneuploidies identify new Williams‐Beuren syndrome patients with atypical deletions

Por Howald, C, Merla, G, Digilio, M C, Amenta, S, Lyle, R, Deutsch, S, Choudhury, U, Bottani, A, Antonarakis, S E, Fryssira, H, Dallapiccola, B, Reymond, A
Publicado em 2006

Expression of base excision repair key factors and miR17 in familial and sporadic breast cancer

Por De Summa, S, Pinto, R, Pilato, B, Sambiasi, D, Porcelli, L, Guida, G, Mattioli, E, Paradiso, A, Merla, G, Micale, L, De Nittis, P, Tommasi, S
Publicado em 2014