Linkage studies on X-linked ichthyosis in Sardinia.

per Filippi, G, Meera Khan, P
Publicat 1968

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

per Rinaldi, A, Filippi, G, Siniscalco, M
Publicat 1976

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

per Rinaldi, A, Archidiacono, N, Rocchi, M, Filippi, G
Publicat 1979

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

per Rocchi, M, Stormi, M, Archidiacono, N, Filippi, G
Publicat 1979

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

per Romeo, G, Rinaldi, A, Urbano, F, Filippi, G
Publicat 1976

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

per Archidiacono, N, Tecilazich, D, Tonini, G, Rocchi, M, Filippi, G
Publicat 1979

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

per D'Angelo, E, De Filippi, G, Rossi, P, Taglietti, V
Publicat 1995

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

per Filippi, G., Rinaldi, A., Palmarino, R., Seravalli, E., Siniscalco, M.
Publicat 1977

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

per Rinaldi, A, Velivasakis, M, Latte, B, Filippi, G, Siniscalco, M
Publicat 1978

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

per Filippi, G, Rinaldi, A, Crisponi, G, Daniels, G L, Siniscalco, M
Publicat 1979

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

per Filippi, G, Pecile, V, Archidiacono, N, Baragino, E, Auber, G, Rocchi, M
Publicat 1983

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

per Filippi, G, Mannucci, P M, Coppola, R, Farris, A, Rinaldi, A, Siniscalco, M
Publicat 1984

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

per Rocchi, M, Archidiacono, N, Rinaldi, A, Filippi, G, Bartolucci, G, Fancello, G S, Siniscalco, M
Publicat 1990

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

per Siniscalco, M., Bernini, L., Filippi, G., Latte, B., Khan, P. Meera, Piomelli, S., Rattazzi, M.
Publicat 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.

per Lenzerini, L, Meera Khan, P, Filippi, G, Rattazzi, M C, Ray, A K, Siniscalco, M
Publicat 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.

per Szabo, P, Purrello, M, Rocchi, M, Archidiacono, N, Alhadeff, B, Filippi, G, Toniolo, D, Martini, G, Luzzatto, L, Siniscalco, M
Publicat 1984

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

per 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.
Publicat a Multidiscip Respir Med (2017)