Pilot Study on Schizophrenia in Sardinia
Ott, Jurg, Macciardi, Fabio, Shen, Yuanyuan, Carta, Mauro G., Murru, Andrea, Triunfo, Riccardo, Robledo, Renato, Rinaldi, Antoniettina, Contu, Licinio, Siniscalco, Marcello
Published in Human heredity (01.01.2010)
Published in Human heredity (01.01.2010)
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Journal Article
Further Data on a 9.1-kb Insertion-Deletion Polymorphism: Survey of Mediterranean Populations
Sidoti, Antonella, Robledo, Renato, Rinaldi, Antoniettina, D'angelo, Rosalia, Rinaldi, Carmela, Amato, Aldo
Published in Human biology (01.06.2006)
Published in Human biology (01.06.2006)
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Journal Article
A 9.1-kb Gap in the Genome Reference Map Is Shown to Be a Stable Deletion/Insertion Polymorphism of Ancestral Origin
Robledo, Renato, Orru, Sandro, Sidoti, Antonella, Muresu, Rosella, Esposito, Diane, Grimaldi, Marie Claude, Carcassi, Carlo, Rinaldi, Antoniettina, Bernini, Luigi, Contu, Licinio, Romani, Massimo, Roe, Bruce, Siniscalco, Marcello
Published in Genomics (San Diego, Calif.) (01.12.2002)
Published in Genomics (San Diego, Calif.) (01.12.2002)
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Journal Article
A Novel Approach to Search for Identity by Descent in Small Samples of Patients and Controls from the Same Mendelian Breeding Unit: A Pilot Study on Myopia
Heath, Simon, Robledo, Renato, Beggs, William, Feola, Gaetano, Parodo, Carlo, Rinaldi, Antoniettina, Contu, Licinio, Dana, Debra, Stambolian, Dwight, Siniscalco, Marcello
Published in Human heredity (01.01.2001)
Published in Human heredity (01.01.2001)
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Journal Article
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect
ROCCHI, M, ARCHIDIACONO, N, RINALDI, A, FILIPPI, G, BARTOLUCCI, G, SANNIO FANCELLO, G, SINISCALCO, M
Published in American journal of human genetics (01.04.1990)
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Published in American journal of human genetics (01.04.1990)
Journal Article
The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD
Webster, C, Filippi, G, Rinaldi, A, Mastropaolo, C, Tondi, M, Siniscalco, M, Blau, H M
Published in Human genetics (01.09.1986)
Published in Human genetics (01.09.1986)
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Journal Article
Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutations
Filippi, G, Arslanian, A, Dagna-Bricarelli, F, Pierluigi, M, Grasso, M, Rinaldi, A, Rocchi, M, Siniscalco, M
Published in American journal of medical genetics (15.09.1991)
Published in American journal of medical genetics (15.09.1991)
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Journal Article
Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region
Robledo, R, Melis, P, Laficara, F, Marchi, J, Rinaldi, A, Siniscalco, M, Filippi, G
Published in American journal of medical genetics (12.07.1996)
Published in American journal of medical genetics (12.07.1996)
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Journal Article
Genetic Variation in the Quantitative Levels of an NADP (H)-Binding Protein (FX) in Human Erythrocytes
Lenzerini, Luciano, Benatti, Umberto, Morelli, Alessandro, Pontremoli, Sandro, Flora, Antonio De, Piazza, Alberto, Rinaldi, Antoniettina, Filippi, Giorgio, Siniscalco, Marcello
Published in Blood (01.02.1981)
Published in Blood (01.02.1981)
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Journal Article
Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: III. Molecular analysis with the StB12.3 probe
Grasso, M, Perroni, L, Dagna-Bricarelli, F, Rinaldi, A, Robledo, R, Siniscalco, M, Filippi, G
Published in American journal of medical genetics (09.08.1996)
Published in American journal of medical genetics (09.08.1996)
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Journal Article
X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies
Robledo, R, Melis, P, Schillinger, E, Casciano, I, Balazs, I, Rinaldi, A, Siniscalco, M, Filippi, G
Published in American journal of medical genetics (06.11.1995)
Published in American journal of medical genetics (06.11.1995)
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Brief report: linkage between G6PD and fragile-X syndrome
Filippi, G, Rinaldi, A, Archidiacono, N, Rocchi, M, Balazs, I, Siniscalco, M
Published in American journal of medical genetics (01.05.1983)
Published in American journal of medical genetics (01.05.1983)
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