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

od Mareni, C, Migeon, B R
Wydane 1981

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

od Mareni, C, Repetto, L, Forteleoni, G, Meloni, T, Gaetani, G F
Wydane 1984

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

od Kirkman, H N, Gaetani, G D, Clemons, E H, Mareni, C
Wydane 1975

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

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

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

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

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

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

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

od 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.
Wydane 2000