T. Tuveri

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First trimester diagnosis of β‐thalassaemia in a twin pregnancy

A. Cao, G. Monni, A. M. Falchi, 1986 .

β° Thalassemia Trait in Sardinia

A. Cao, R. Galanello, L. Maccioni, 1979 .

Beta 0 thalassemia trait in Sardinia.

A. Cao, R. Galanello, L. Maccioni, 1979, Hemoglobin.

Heterozygous β‐thalassemia: Relationship between the hematological phenotype and the type of β‐thalassemia mutation

A. Cao, A. Mosca, R. Galanello, 1992 .

Molecular screening and fetal diagnosis of β-thalassemia in the Italian population

A. Cao, G. Monni, A. Meloni, 1992, Human Genetics.

Phenotypic effect of heterozygous α and β-Thalassemia interaction

M. Pirastu, A. Cao, R. Galanello, 1983 .

Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia.

A. Cao, R. Galanello, E. Paglietti, 1981, American journal of human genetics.

Phenotypic Effect of Heterozygous a and $ # { 176 }-Thalassemia Interaction

Renzo, A. Cao, Melis, 2005 .

Molecular mechanism accounting for milder types of thalassemia major.

A. Meloni, A. Cao, A. M. Falchi, 1983, The Journal of pediatrics.

Antenatal Diagnosis of β‐Thalassemia in Sardinia a

A. Cao, R. Galanello, M. Rosatelli, 1990 .

Prenatal diagnosis ofv thalassaemia by oligonucleotide analysis inMediterranean populations

A. Cao, G. Monni, A. Di Tucci, 1988 .

Problems in prenatal diagnosis of β‐thalassaemia by fetal blood analysis: β‐chain variant comigrating with gamma chains

A. Cao, G. Monni, A. Di Tucci, 1988 .

Pitfalls in genetic counselling for β‐thalassemia: an individual with 4 different thalassemia mutations

A. Cao, R. Galanello, M. Addis, 1988, Clinical genetics.

Prenatal diagnosis of thalassemia major by fetal blood analysis: Experience with 1000 cases

G. Monni, A. M. Falchi, C. Rosatelli, 1986, Prenatal diagnosis.

Antenatal Diagnosis of Thalassemia Major in Sardinia a

M. Pirastu, A. Cao, G. Monni, 1985, Annals of the New York Academy of Sciences.

PRENATAL DIAGNOSIS OF BETA-THALASSAEMIA WITH THE SYNTHETIC-OLIGOMER TECHNIQUE

A. Cao, G. Monni, A. M. Falchi, 1985, The Lancet.

Prenatal Diagnosis of β-Thalassemia by the Analysis of Trophoblast DNA with the Synthetic Oligomer Technique

A. Cao, G. Monni, C. Rosatelli, 1985 .

Hematological phenotype of the double heterozygous state for alpha and beta thalassemia.

A. Cao, A. M. Falchi, M. Furbetta, 1984, Hemoglobin.

Beta-Thalassaemia types in southern Sardinia.

A. Cao, R. Galanello, A. M. Falchi, 1981, Journal of medical genetics.

Fetal HLA typing in β thalassaemia: implications for haemopoietic stem-cell transplantation

A. Cao, P. Cossu, M. Lai, 2003, The Lancet.

Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction.

M. Pirastu, A. Cao, R. Galanello, 1983, Blood.

The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population.

Y. Kan, M. Pirastu, A. Cao, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Diagnosis of the β0 Thalassemia Trait at Birth

A. Cao, A. M. Falchi, M. Furbetta, 1981 .

Thalassemia intermedia resulting from a mild beta-thalassemia mutation.

L. Oggiano, A. Massa, P. Pistidda, 1989, Blood.

Haematological and obstetric aspects of antenatal diagnosis of beta-thalassaemia: experience with 200 cases.

A. Cao, A. M. Falchi, M. Furbetta, 1982, Journal of medical genetics.

Prevention of homozyous /-thalassemia by carrier screening and prenatal diagnosis in Sardinia

A. Cao, R. Galanello, E. Paglietti, 1981 .

Prenatal Diagnosis of β Thalassaemia by Fetal Red Cell Enrichment with NH4Cl‐NH4HCO3 Differential Lysis of Maternal Cells

A. Cao, M. Furbetta, C. Rosatelli, 1980, British journal of haematology.

Prenatal diagnosis of thalassaemia major resulting from Lepore/ beta-thalassaemia genotype.

A. Cao, A. M. Falchi, M. Furbetta, 1981, Journal of medical genetics.

r-thalassaemia types insouthern Sardinia

A. Cao, R. Galanello, A. M. Falchi, 1981 .

P-thalassaemia types in southern Sardinia

A. M. Falchi, L. Maccioni, M. Melis, 2022 .

Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia.

A. Cao, R. Galanello, E. Paglietti, 1982, Birth defects original article series.

Two new β-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention

J. Traeger-Synodinos, E. Kanavakis, R. Galanello, 2009, Haematologica.

Prenatal diagnosis of beta-thalassaemia by fetal red cell concentration with anti-AB serum.

A. Cao, P. Fioretti, M. Furbetta, 1979, Journal of medical genetics.

Prenatal diagnosis of3-thalassaemia byfetal redcell concentration withanti-AB serum1

A. Cao, P. Fioretti, M. Furbetta, 1979 .

Prenatal diagnosis of 3-thalassaemia by fetal red cell concentration with anti-AB serum1

A. Cao, P. Fioretti, M. Furbetta, 2022 .

Beta thalassaemia mutations in Sardinians: implications for prenatal diagnosis.

A. Cao, A. Di Tucci, C. Rosatelli, 1987, Journal of medical genetics.

Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutation.

A. Cao, A. Mosca, R. Galanello, 1992, American journal of hematology.

A case of the orocraniodigital (Juberg-Hayward) syndrome

A. Cao, A. M. Falchi, N. Tannoia, 2022 .

DIFFICULTIES IN ANTENATAL DIAGNOSIS OF INHERITED HAEMOGLOBINOPATHIES: γ‐CHAIN VARIANTS

A. Cao, A. M. Falchi, M. Furbetta, 1981 .

Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNA.

G. Loudianos, A. Cao, G. Monni, 1990, Journal of Medical Genetics.