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A Cao

Showing results (181-190 of 461) with videos related to

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Human Genetics|September 1, 1990
Molecular bases for cystic fibrosis in the Sardinian populationG B Leoni, C Rosatelli, R Sardu, et al.
Haematologica|March 26, 1999
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemiaR Galanello, M D Cipollina, C Dessì, 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.
Human Mutation|February 16, 2005
Two novel mutations of the AIRE protein affecting its homodimerization propertiesA Meloni, E Fiorillo, D Corda, et al.
Journal of the Neurological Sciences|February 1, 1978
Schwartz-Jampel syndrome. Clinical, electrophysiological and histopathological study of a severe variantA Cao, C Cianchetti, L Calisti, et al.
Blood|July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interactionM A Melis, M Pirastu, R Galanello, et al.
Acta Haematologica|January 1, 1990
High-dose intravenous immunoglobulin in the management of autoimmune hemolytic anemia complicating thalassemia majorF Argiolu, G Diana, M Arnone, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1996
Deletion in the peripherin/RDS gene in two unrelated Sardinian families with autosomal dominant butterfly-shaped macular dystrophyM Fossarello, C Bertini, M S Galantuomo, et al.
Pediatric Research|November 1, 1981
Glucose-6-phosphate dehydrogenase red blood cell phenotype in GdMediterranean heterozygous females and hemizygous males at birthG Sanna, F Frau, S De Virgiliis, et al.
Pageof 47

Showing results (181-190 of 461) with videos related to

Sort By:
Pageof 47
Human Genetics|September 1, 1990
Molecular bases for cystic fibrosis in the Sardinian populationG B Leoni, C Rosatelli, R Sardu, et al.
Haematologica|March 26, 1999
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemiaR Galanello, M D Cipollina, C Dessì, 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.
Human Mutation|February 16, 2005
Two novel mutations of the AIRE protein affecting its homodimerization propertiesA Meloni, E Fiorillo, D Corda, et al.
Journal of the Neurological Sciences|February 1, 1978
Schwartz-Jampel syndrome. Clinical, electrophysiological and histopathological study of a severe variantA Cao, C Cianchetti, L Calisti, et al.
Blood|July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interactionM A Melis, M Pirastu, R Galanello, et al.
Acta Haematologica|January 1, 1990
High-dose intravenous immunoglobulin in the management of autoimmune hemolytic anemia complicating thalassemia majorF Argiolu, G Diana, M Arnone, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1996
Deletion in the peripherin/RDS gene in two unrelated Sardinian families with autosomal dominant butterfly-shaped macular dystrophyM Fossarello, C Bertini, M S Galantuomo, et al.
Pediatric Research|November 1, 1981
Glucose-6-phosphate dehydrogenase red blood cell phenotype in GdMediterranean heterozygous females and hemizygous males at birthG Sanna, F Frau, S De Virgiliis, et al.
Pageof 47