A. Rinaldi

发表

Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm

R. Nussbaum, M. Purrello, S. Traccis, 2004, Human Genetics.

W. Rutter, S. Naylor, F. Grosveld, 2012 .

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

P. Mannucci, R. Coppola, M. Siniscalco, 1984, American journal of human genetics.

Combination of old and new strategies for the molecular mapping of the human X-chromosome.

P. Szabo, M. Siniscalco, G. Filippi, 1982, Progress in clinical and biological research.

Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.

R. Palmarino, G Filippi, A Rinaldi, 1977, Genetics.

Brief report: linkage between G6PD and fragile-X syndrome.

N. Archidiacono, M. Rocchi, I. Balazs, 1983, American journal of medical genetics.

A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin.

B. Roe, C. Carcassi, L. Contu, 2002, Genomics.

Pilot Study on Schizophrenia in Sardinia

J. Ott, L. Contu, Yuanyuan Shen, 2010, Human Heredity.

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.

M. Rocchi, M. Pierluigi, M. Grasso, 1991, American journal of medical genetics.

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

G. Romeo, G. Filippi, F. Urbano, 1976, American journal of human genetics.

Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: III. Molecular analysis with the StB12.3 probe.

L. Perroni, M. Grasso, M. Siniscalco, 1996, American journal of medical genetics.

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

N. Archidiacono, M. Rocchi, G. Bartolucci, 1990, American journal of human genetics.

The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation

H. Blau, M. Siniscalco, M. Tondi, 1986, Human Genetics.

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

M. Siniscalco, G. Filippi, A. Rinaldi, 1976, American journal of human genetics.

Is the gene for steroid sulfatase x-linked in man? an appraisal of data from humans, mice, and their hybrids. Abstr.

M. Rocchi, M. Purrello, I. Balazs, 1982 .

G6PD AS A TOOL AND A TARGET FOR STUDIES ON X-CHROMOSOME LINKAGE1

M. Purrello, M. Siniscalco, G. Filippi, 1986 .

Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum.

R. Nagel, C. Raventós-Suárez, A. Rinaldi, 1983, Proceedings of the National Academy of Sciences of the United States of America.

A case of Edward's syndrome with pseudodicentric isochromosome 18: 46,XY,i dic(18) (p11::p11).

V. Ventruto, C. Trapassi, L. Pagano, 1982, Annales de genetique.

X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies.

I. Balazs, I. Casciano, M. Siniscalco, 1995, American journal of medical genetics.

Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region.

J. Marchi, M. Siniscalco, P. Melis, 1996, American journal of medical genetics.

(FX) in human erythrocytes Genetic variation in the quantitative levels of an NADP (H)-binding protein

A. Morelli, S. Pontremoli, U. Benatti, 2011 .

Genetic variation in the quantitative levels of an NADP (H)-binding protein (FX) in human erythrocytes

A. Morelli, S. Pontremoli, U. Benatti, 1981 .

Genetic variation in the quantitative levels of an NADP (H)-binding protein (FX) in human erythrocytes.

A. De Flora, A. Morelli, S. Pontremoli, 1981, Blood.

(G6PD and Deutan)

Giorgio, M. Siniscalco, Filippi, 2006 .

The effect of pyrroline-5-carboxylic acid on nucleotide metabolism in erythrocytes from normal and glucose-6-phosphate dehydrogenase-deficient subjects.

R. Nagel, G. C. Yeh, J. Phang, 1984, The Journal of biological chemistry.

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

L. Contu, William Beggs, M. Siniscalco, 2001, Human Heredity.

The effect of X chromosome inactivation on the inhibition of Plasmodium falciparum malaria growth by glucose-6-phosphate-dehydrogenase- deficient red cells

C. Suarez, R. Nagel, E. Roth, 1983 .

The effect of X chromosome inactivation on the inhibition of Plasmodium falciparum malaria growth by glucose-6-phosphate-dehydrogenase-deficient red cells.

R. Nagel, A. Rinaldi, E. Roth, 1983, Blood.

The laboratory use of butylnitrite for the production of methemoglobin

G. Filippi, G. M. Fiori, A. Rinaldi, 1985, American journal of hematology.