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Genetic Testing|September 25, 1999
A strategy for fragile-X carrier screeningM A Melis, M Addis, C Lepiani, et al.Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.American Journal of Hematology|October 1, 1988
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin geneR Galanello, E Paglietti, M A Melis, et al.Clinical Genetics|March 1, 1988
Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutationsR Galanello, M E Paglietti, M Addis, et al.Developmental Medicine and Child Neurology|January 1, 1993
Diagnosis of DMD carrier status in a family with no known affected malesF Muntoni, A Mateddu, M Cau, et al.British Journal of Haematology|April 1, 1983
Alpha globin gene analysis in a Sardinian family with interacting alpha and beta thalassaemia genesM A Melis, R Galanello, A CaoHemoglobin|January 1, 1979
Beta 0 thalassemia trait in SardiniaR Galanello, M A Melis, R Ruggeri, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Clinical presentation of thalassemia major due to homozygous beta (0)-thalassemiaR Galanello, P Cossu, M Pirastu, et al.Acta Haematologica|January 1, 1977
Quantitation of Hb a2 with DE-52 microchromatography in whole blood as screening test for beta-thalassemia heterozygotesR Galanello, M A Melis, P Muroni, et al.Hemoglobin|January 1, 1984
Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J SardegnaL Maccioni, R Galanello, M A Melis, et al.Pageof 43