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Journal of Medical Genetics|December 1, 1978
Thalassaemia types and their incidence in SardiniaA Cao, R Galanello, M Furbetta, et al.Clinical Genetics|July 1, 1985
Genetic counseling and genetic heterogeneity in the thalassemiasE Paglietti, R Galanello, M Addis, et al.Prenatal Diagnosis|September 1, 1987
Chorionic villus sampling and acceptance rate of prenatal diagnosisA Cao, P Cossu, G Monni, et al.Humangenetik|September 20, 1975
A case of extra small acrocentric bisatellited chromosome in a non mongoloid childM Furbetta, G Rosi, M Biagioni, et al.Pediatric Research|February 1, 1984
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2R Galanello, M A Melis, L Maccioni, et al.Acta Haematologica|January 1, 1984
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotypeR Galanello, E Paglietti, M A Melis, et al.Progress in Clinical and Biological Research|January 1, 1989
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian familyR Galanello, A Podda, M A Melis, et al.American Journal of Human Genetics|July 1, 1981
Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in SardiniaA Cao, M Furbetta, R Galanello, et al.Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.Clinical Genetics|May 1, 1993
Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counsellingM A Melis, M Cau, R Congiu, et al.Pageof 43