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Bailliere'S Clinical Haematology|June 29, 2000
Prenatal diagnosis and screening of the haemoglobinopathiesA Cao, R Galanello, M C RosatelliCiba Foundation Symposium|January 1, 1996
Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experienceA Cao, M C Rosatelli, R GalanelloBlood Reviews|March 1, 1994
Genotype-phenotype correlations in beta-thalassemiasA Cao, R Galanello, M C RosatelliCurrent Opinion in Genetics & Development|June 1, 1991
Population-based genetic screeningA Cao, M C Rosatelli, R GalanelloJAMA|October 23, 1997
Molecular diagnosis and carrier screening for beta thalassemiaA Cao, L Saba, R Galanello, et al.Journal of Medical Genetics|April 1, 1984
A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermediaR Galanello, L Maccioni, M C Rosatelli, et al.British Journal of Haematology|June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemiaM C Rosatelli, V Faà, A Meloni, et al.British Journal of Haematology|August 1, 1989
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemiaR Galanello, S Barella, L Maccioni, et al.Bailliere'S Clinical Haematology|March 1, 1993
Screening and prenatal diagnosis of the haemoglobinopathiesA Cao, M C RosatelliAnnals of the New York Academy of Sciences|January 1, 1990
Antenatal diagnosis of beta-thalassemia in SardiniaA Cao, M C Rosatelli, G B Leoni, et al.Pageof 40