Taq I RFLP in the human cellular retinol-binding protein (CRBP) gene.

অনুযায়ী Pellegrino, A, Garofalo, S, Cocozza, S, Monticelli, A, Faraonio, R, Varrone, S, Colantuoni, V
প্রকাশিত 1988

The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.

অনুযায়ী Filla, A., De Michele, G., Cavalcanti, F., Pianese, L., Monticelli, A., Campanella, G., Cocozza, S.
প্রকাশিত 1996

Eco RI RFLP in the human IGF II gene.

অনুযায়ী Cocozza, S, Garofalo, S, Robledo, R, Monticelli, A, Conti, A, Chiarotti, L, Frunzio, R, Bruni, C B, Varrone, S
প্রকাশিত 1988

Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype

অনুযায়ী Giacchetti, M, Monticelli, A, De Biase, I, Pianese, L, Turano, M, Filla, A, De Michele, G, Cocozza, S
প্রকাশিত 2004

The effect of parental gender on the GAA dynamic mutation in the FRDA gene.

অনুযায়ী Pianese, L, Cavalcanti, F, De Michele, G, Filla, A, Campanella, G, Calabrese, O, Castaldo, I, Monticelli, A, Cocozza, S
প্রকাশিত 1997

Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers

অনুযায়ী Pianese, L, Turano, M, Lo, C, De Biase, I, Giacchetti, M, Monticelli, A, Criscuolo, C, Filla, A, Cocozza, S
প্রকাশিত 2004

Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.

অনুযায়ী Pianese, L, Cocozza, S, Campanella, G, Castaldo, I, Cavalcanti, F, De Michele, G, Filla, A, Monticelli, A, Munaro, M, Redolfi, E
প্রকাশিত 1994

Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich's ataxia

অনুযায়ী Santoro, L, De Michele, G, Perretti, A, Crisci, C, Cocozza, S, Cavalcanti, F, Ragno, M, Monticelli, A, Filla, A, Caruso, G
প্রকাশিত 1999

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

অনুযায়ী De Michele, G, Filla, A, Cavalcanti, F, Di Maio, L, Pianese, L, Castaldo, I, Calabrese, O, Monticelli, A, Varrone, S, Campanella, G
প্রকাশিত 1994

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.

অনুযায়ী De Michele, G, De Fusco, M, Cavalcanti, F, Filla, A, Marconi, R, Volpe, G, Monticelli, A, Ballabio, A, Casari, G, Cocozza, S
প্রকাশিত 1998