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M A Melis

Showing results (21-30 of 58) with videos related to

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American Journal of Medical Genetics. Part A|June 11, 2005
New case of contiguous gene syndrome at chromosome 8p11.2p12M Cau, R Congiu, R Origa, et al.
Haematologica|May 1, 1985
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotypeR Galanello, E Paglietti, N Giagu, et al.
British Journal of Haematology|April 1, 1980
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype levelG Sanna, F Frau, M A Melis, et al.
British Journal of Haematology|December 1, 1983
Phenotypic manifestations of heterozygous non-deletion alpha-thalassaemia (alpha alpha/(alpha alpha)th) in SardiniansR Galanello, E Paglietti, L Giagu, et al.
British Journal of Haematology|February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian familiesM Furbetta, R Galanello, A Ximenes, et al.
Human Mutation|January 8, 2000
Two novel mutations (10410 T-->G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Mutations in brief no. 149. OnlineM Cau, A Cao, D Loi, et al.
Minerva Medica|March 17, 1981
[Our experience in screening and genetic counseling for beta-thalassemia]A Cao, R Galanello, M A Melis, et al.
Journal of Medical Genetics|October 1, 1980
alpha-Thalassaemia in Sardinian infantsR Galanello, G Diana, M Furbetta, et al.
Blood|January 15, 1991
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathyA Podda, R Galanello, L Maccioni, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|June 11, 2005
New case of contiguous gene syndrome at chromosome 8p11.2p12M Cau, R Congiu, R Origa, et al.
Haematologica|May 1, 1985
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotypeR Galanello, E Paglietti, N Giagu, et al.
British Journal of Haematology|April 1, 1980
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype levelG Sanna, F Frau, M A Melis, et al.
British Journal of Haematology|December 1, 1983
Phenotypic manifestations of heterozygous non-deletion alpha-thalassaemia (alpha alpha/(alpha alpha)th) in SardiniansR Galanello, E Paglietti, L Giagu, et al.
British Journal of Haematology|February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian familiesM Furbetta, R Galanello, A Ximenes, et al.
Human Mutation|January 8, 2000
Two novel mutations (10410 T-->G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Mutations in brief no. 149. OnlineM Cau, A Cao, D Loi, et al.
Minerva Medica|March 17, 1981
[Our experience in screening and genetic counseling for beta-thalassemia]A Cao, R Galanello, M A Melis, et al.
Journal of Medical Genetics|October 1, 1980
alpha-Thalassaemia in Sardinian infantsR Galanello, G Diana, M Furbetta, et al.
Blood|January 15, 1991
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathyA Podda, R Galanello, L Maccioni, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
Pageof 6