Linkage studies on X-linked ichthyosis in Sardinia.

di Filippi, G, Meera Khan, P
Pubblicazione 1968

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

di Rinaldi, A, Filippi, G, Siniscalco, M
Pubblicazione 1976

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

di Rinaldi, A, Archidiacono, N, Rocchi, M, Filippi, G
Pubblicazione 1979

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

di Rocchi, M, Stormi, M, Archidiacono, N, Filippi, G
Pubblicazione 1979

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

di Romeo, G, Rinaldi, A, Urbano, F, Filippi, G
Pubblicazione 1976

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

di Archidiacono, N, Tecilazich, D, Tonini, G, Rocchi, M, Filippi, G
Pubblicazione 1979

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

di D'Angelo, E, De Filippi, G, Rossi, P, Taglietti, V
Pubblicazione 1995

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

di Filippi, G., Rinaldi, A., Palmarino, R., Seravalli, E., Siniscalco, M.
Pubblicazione 1977

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

di Rinaldi, A, Velivasakis, M, Latte, B, Filippi, G, Siniscalco, M
Pubblicazione 1978

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

di Filippi, G, Rinaldi, A, Crisponi, G, Daniels, G L, Siniscalco, M
Pubblicazione 1979

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

di Filippi, G, Pecile, V, Archidiacono, N, Baragino, E, Auber, G, Rocchi, M
Pubblicazione 1983

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

di Filippi, G, Mannucci, P M, Coppola, R, Farris, A, Rinaldi, A, Siniscalco, M
Pubblicazione 1984

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

di Rocchi, M, Archidiacono, N, Rinaldi, A, Filippi, G, Bartolucci, G, Fancello, G S, Siniscalco, M
Pubblicazione 1990

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

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

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

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

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

di 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.
Pubblicato in Multidiscip Respir Med (2017)