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Circulating 'trophoblast' cells in pregnancy have maternal genetic markers 1-gen-1989 Bertero, Mt; Camaschella, Clara; Serra, A; Bergui, L; Caligaris Cappio, F.
A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer 1-gen-1990 Camaschella, Clara; Serra, A; Gottardi, E; Alfarano, A; Revello, D; Mazza, U; Saglio, G.
The homozygous state for the -87 C----G beta + thalassaemia 1-gen-1990 Camaschella, Clara; Alfarano, A; Gottardi, E; Serra, A; Revello, D; Saglio, G.
The C->T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta-thalassemia in the Italian population 1-gen-1990 Ristaldi, Ms; Murru, S; Loudianos, G; Casula, L; Porcu, S; Pigheddu, D; Fanni, B; Sciarratta, Gv; Agosti, S; Parodi, Mi; Leone, D; Camaschella, Clara; Serra, A; Pirastu, M; Cao, A.
Thrombotic thrombocytopenic purpura in pregnancy with maternal and fetal survival. Case report 1-gen-1990 Maina, A; Donvito, V; Giachino, O; Stratta, P; Camaschella, Clara
Haplotype distribution and molecular defects of PKU in Italy 1-gen-1990 Dianzani, I; Camaschella, Clara; Saglio, G; Ferrero, Gb; Romeo, G; Devoto, M; Romano, C; Cerone, R; Giovannini, M; Riva, E; Trefz, Fk; Lichter Konechi, U; Woo, Sl
Prenatal Diagnosis of fetal hemoglobin Lepore-Boston Disease on maternal peripheral blood 1-gen-1990 Camaschella, Clara; Alfarano, A; Gottardi, E; Travi, M; Primignani, P; Caligaris Cappio, F; Saglio, G.
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy 1-gen-1990 Dianzani, I; Devoto, M; Camaschella, Clara; Saglio, G; Ferrero, Gb; Cerone, R; Romano, C; Romeo, G; Giovannini, M; Riva, E; Angeneydt, F; Trefz, Fk; Okano, Y; Woo, Slc
Molecular characterization of Black HPFH type I in a patient from Cuba 1-gen-1990 Martinez, G; Hernandez, A; Corral, L; Muniz, A; Alaez, C; Serra, A; Alfarano, A; Saglio, G; Camaschella, Clara
Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic origin 1-gen-1990 Alfarano, A; Gottardi, E; Serra, A; Piga, A; Mandrino, M; Mazza, U; Camaschella, Clara
Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis 1-gen-1990 Gottardi, E; Alfarano, A; Serra, A; Sciarratta, G; Bertero, Mt; Saglio, G; Camaschella, Clara
A newly characterized alpha-thalassemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian family 1-gen-1991 Fortina, P; Dianzani, I; Serra, A; Gottardi, E; Saglio, G; Farinasso, L; Piga, A; Gabutti, V; Camaschella, Clara
A spontaneous mutation causing unstable Hb Hammersmith: detection of the alpha 42 TTT->TCT change by CCM and direct sequencing 1-gen-1991 Dianzani, I; Ramus, S; Cotton, Rgh; Camaschella, Clara
Molecular -thalassemia intermedia in patients of Italian descent andcharacterization of -thalassemia mutations.identification of three novel 1-gen-1991 Murru, S; Loudianos, G; Deiana, M; Camaschella, Clara; Sciarratta, Gv; Agosti, S; Parodi, Mi; Cerruti, P; Cao, A; Pirastu, M.
Heterozygotes identification by chemical cleavage of mismatch 1-gen-1991 Dianzani, I; Forrest, Sm; Camaschella, Clara; Gottardi, E; Cotton, Rgh
Screening for mutations in the phenylalanine hydroxylase gene in Italian PKU patients using the Chemical cleavage method: a new splice mutation 1-gen-1991 Dianzani, I; Forrest, Sm; Camaschella, Clara; Saglio, G; Ponzone, A; Cotton, Rgh
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatch 1-gen-1991 Dianzani, I; Camaschella, Clara; Saglio, G; Forrest, Sm; Ramus, S; Cotton, Rgh
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis 1-gen-1992 Iolascon, A; Miraglia Del Giudice, E; Camaschella, Clara
Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFH 1-gen-1992 Gottardi, E; Losekoot, M; Fodde, R; Saglio, G; Camaschella, Clara; Bernini, Lf
Molecular characterization and functional studies on Hb Kempsey, beta 99 (G-1) ASP->ASN, a high-oxygen affinity variant 1-gen-1992 Ricco, G; Scaroina, F; Amprino, Mc; Gottardi, E; Parziale, A; Alfarano, A; Camaschella, Clara
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