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American Journal of Medical Genetics. Part A
|
June 11, 2005
New case of contiguous gene syndrome at chromosome 8p11.2p12
M Cau, R Congiu, R Origa, et al.
Haematologica
|
May 1, 1985
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype
R 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 level
G 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 Sardinians
R Galanello, E Paglietti, L Giagu, et al.
British Journal of Haematology
|
February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian families
M 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. Online
M 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 infants
R Galanello, G Diana, M Furbetta, et al.
Blood
|
January 15, 1991
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy
A 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 bodies
D Gasperini, R Galanello, M A Melis, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 58) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics. Part A
|
June 11, 2005
New case of contiguous gene syndrome at chromosome 8p11.2p12
M Cau, R Congiu, R Origa, et al.
Haematologica
|
May 1, 1985
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype
R 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 level
G 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 Sardinians
R Galanello, E Paglietti, L Giagu, et al.
British Journal of Haematology
|
February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian families
M 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. Online
M 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 infants
R Galanello, G Diana, M Furbetta, et al.
Blood
|
January 15, 1991
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy
A 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 bodies
D Gasperini, R Galanello, M A Melis, et al.
Page
of 6