Linkage studies on X-linked ichthyosis in Sardinia.

nork Filippi, G, Meera Khan, P
Argitaratua 1968

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

nork Rinaldi, A, Filippi, G, Siniscalco, M
Argitaratua 1976

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

nork Rinaldi, A, Archidiacono, N, Rocchi, M, Filippi, G
Argitaratua 1979

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

nork Rocchi, M, Stormi, M, Archidiacono, N, Filippi, G
Argitaratua 1979

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

nork Romeo, G, Rinaldi, A, Urbano, F, Filippi, G
Argitaratua 1976

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

nork Archidiacono, N, Tecilazich, D, Tonini, G, Rocchi, M, Filippi, G
Argitaratua 1979

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

nork D'Angelo, E, De Filippi, G, Rossi, P, Taglietti, V
Argitaratua 1995

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

nork Filippi, G., Rinaldi, A., Palmarino, R., Seravalli, E., Siniscalco, M.
Argitaratua 1977

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

nork Rinaldi, A, Velivasakis, M, Latte, B, Filippi, G, Siniscalco, M
Argitaratua 1978

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

nork Filippi, G, Rinaldi, A, Crisponi, G, Daniels, G L, Siniscalco, M
Argitaratua 1979

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

nork Filippi, G, Pecile, V, Archidiacono, N, Baragino, E, Auber, G, Rocchi, M
Argitaratua 1983

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

nork Filippi, G, Mannucci, P M, Coppola, R, Farris, A, Rinaldi, A, Siniscalco, M
Argitaratua 1984

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

nork Rocchi, M, Archidiacono, N, Rinaldi, A, Filippi, G, Bartolucci, G, Fancello, G S, Siniscalco, M
Argitaratua 1990

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

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

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

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

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

nork 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.
Argitaratua izan da Multidiscip Respir Med (2017)