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M A Melis

Showing results (11-20 of 58) with videos related to

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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.
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.
Blood|July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interactionM A Melis, M Pirastu, R Galanello, et al.
Human Genetics|August 1, 1993
Identification of a novel T-insertion polymorphism at the DMD locusF Muntoni, M Cau, R Congiu, et al.
Genetic Testing|September 25, 1999
A strategy for fragile-X carrier screeningM A Melis, M Addis, C Lepiani, et al.
Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.
Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.
Acta Haematologica|January 1, 1983
Serum ferritin levels in hemoglobin H diseaseR Galanello, M A Melis, E Paglietti, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
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.
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.
Blood|July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interactionM A Melis, M Pirastu, R Galanello, et al.
Human Genetics|August 1, 1993
Identification of a novel T-insertion polymorphism at the DMD locusF Muntoni, M Cau, R Congiu, et al.
Genetic Testing|September 25, 1999
A strategy for fragile-X carrier screeningM A Melis, M Addis, C Lepiani, et al.
Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.
Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.
Acta Haematologica|January 1, 1983
Serum ferritin levels in hemoglobin H diseaseR Galanello, M A Melis, E Paglietti, et al.
Pageof 6