Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase.

per Mareni, C, Migeon, B R
Publicat 1981

Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency.

per Mareni, C, Repetto, L, Forteleoni, G, Meloni, T, Gaetani, G F
Publicat 1984

Red cell NADP+ and NADPH in glucose-6-phosphate dehydrogenase deficiency.

per Kirkman, H N, Gaetani, G D, Clemons, E H, Mareni, C
Publicat 1975

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of...

per Pai, G S, Sprenkle, J A, Do, T T, Mareni, C E, Migeon, B R
Publicat 1980

Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)

per Stella, A, Resta, N, Gentile, M, Susca, F, Mareni, C, Montera, M P, Guanti, G
Publicat 1993

A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family

per Montera, M., Piaggio, F., Marchese, C., Gismondi, V., Stella, A., Resta, N., Varesco, L., Guanti, G., Mareni, C.
Publicat 2001

Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients

per MONTERA, M., RESTA, N., SIMONE, C., GUANTI, G., MARCHESE, C., CIVITELLI, S., MANCINI, A., POZZI, S., DE SALVO, L., BRUZZONE, D., DONADINI, A., ROMIO, L., MARENI, C.
Publicat 2000