Linkage studies on X-linked ichthyosis in Sardinia.

Por Filippi, G, Meera Khan, P
Publicado em 1968

Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.

Por Rinaldi, A, Filippi, G, Siniscalco, M
Publicado em 1976

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.

Por Rinaldi, A, Archidiacono, N, Rocchi, M, Filippi, G
Publicado em 1979

Extra small metacentric chromosome identified as i(18p).

Por Rocchi, M, Stormi, M, Archidiacono, N, Filippi, G
Publicado em 1979

Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).

Por Romeo, G, Rinaldi, A, Urbano, F, Filippi, G
Publicado em 1976

Trisomy 20p from maternal t(3;20) translocation.

Por Archidiacono, N, Tecilazich, D, Tonini, G, Rocchi, M, Filippi, G
Publicado em 1979

Synaptic excitation of individual rat cerebellar granule cells in situ: evidence for the role of NMDA receptors.

Por D'Angelo, E, De Filippi, G, Rossi, P, Taglietti, V
Publicado em 1995

Linkage Disequilibrium for Two X-Linked Genes in Sardinia and Its Bearing on the Statistical Mapping of the Human X Chromosome

Por Filippi, G., Rinaldi, A., Palmarino, R., Seravalli, E., Siniscalco, M.
Publicado em 1977

Triplo-X constitution of mother explains apparent occurrence of two recombinants in sibship segregating at two closely X-linked loci (G6PD and deutan).

Por Rinaldi, A, Velivasakis, M, Latte, B, Filippi, G, Siniscalco, M
Publicado em 1978

X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.

Por Filippi, G, Rinaldi, A, Crisponi, G, Daniels, G L, Siniscalco, M
Publicado em 1979

X chromosome replication patterns in a case of X;9 balanced translocation.

Por Filippi, G, Pecile, V, Archidiacono, N, Baragino, E, Auber, G, Rocchi, M
Publicado em 1983

Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.

Por Filippi, G, Mannucci, P M, Coppola, R, Farris, A, Rinaldi, A, Siniscalco, M
Publicado em 1984

Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.

Por Rocchi, M, Archidiacono, N, Rinaldi, A, Filippi, G, Bartolucci, G, Fancello, G S, Siniscalco, M
Publicado em 1990

Population genetics of haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency, with particular reference to the malaria hypothesis

Por Siniscalco, M., Bernini, L., Filippi, G., Latte, B., Khan, P. Meera, Piomelli, S., Rattazzi, M.
Publicado em 1966

Characterization of glucose-6-phosphate dehydrogenase variants. I. Occurrence of a G6PD Seattle-like variant in Sardinia and its interaction with the G6PD Mediterranean variant.

Por Lenzerini, L, Meera Khan, P, Filippi, G, Rattazzi, M C, Ray, A K, Siniscalco, M
Publicado em 1969

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.

Por Szabo, P, Purrello, M, Rocchi, M, Archidiacono, N, Alhadeff, B, Filippi, G, Toniolo, D, Martini, G, Luzzatto, L, Siniscalco, M
Publicado em 1984

Implementation of GOLD consensus report in real life: results from the Velletri-Lariano (VELA) cohort

Por De Filippi, G., Lallini, M., De Riggi, G., Marchetti, G., Dimartino, C. M., Russetti, A. M., Ferrari, E., Pistelli, R., Magnoni, M. S., Riparbelli, M., Rizzi, A., Angeletti, P.
Publicado no Multidiscip Respir Med (2017)