C Camaschella|P Gasparini - JoVE Visualize

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Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 1995

Characterization of mitochondrial DNA in primary cardiomyopathiesA Bobba, S Giannattasio, A Pucci, et al.

Haematologica|August 16, 2000

Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietinM De Gobbi, P Pasquero, F Brunello, et al.

Blood|August 9, 2001

Natural history of congenital dyserythropoietic anemia type IIA Iolascon, J Delaunay, S N Wickramasinghe, et al.

Human Mutation|November 26, 1999

Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, ItalyI Dianzani, U Landegren, C Camaschella, et al.

British Journal of Haematology|April 1, 1992

Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFHE Gottardi, M Losekoot, R Fodde, et al.

British Journal of Haematology|May 1, 1976

Clinical and haematological data in 254 cases of beta-thalassaemia trait in ItalyU Mazza, G Saglio, F C Cappio, et al.

American Journal of Human Genetics|March 1, 1991

Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, et al.

Experimental and Clinical Immunogenetics|January 1, 1993

Identification of a new DNA polymorphism tightly linked to DQ-alpha locusP Gasparini, A Bonizzato, A Totaro, et al.

Science (New York, N.Y.)|November 17, 2001

Seismic evidence of an extended magmatic sill under Mt. VesuviusE Auger, P Gasparini, J Virieux, et al.

Human Mutation|January 1, 1994

Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutationsL Bisceglia, A Grifa, L Zelante, et al.

Pageof 25

Showing results (41-50 of 250) with videos related to

Sort By:

Pageof 25

Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 1995

Characterization of mitochondrial DNA in primary cardiomyopathiesA Bobba, S Giannattasio, A Pucci, et al.

Haematologica|August 16, 2000

Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietinM De Gobbi, P Pasquero, F Brunello, et al.

Blood|August 9, 2001

Natural history of congenital dyserythropoietic anemia type IIA Iolascon, J Delaunay, S N Wickramasinghe, et al.

Human Mutation|November 26, 1999

Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, ItalyI Dianzani, U Landegren, C Camaschella, et al.

British Journal of Haematology|April 1, 1992

Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFHE Gottardi, M Losekoot, R Fodde, et al.

British Journal of Haematology|May 1, 1976

Clinical and haematological data in 254 cases of beta-thalassaemia trait in ItalyU Mazza, G Saglio, F C Cappio, et al.

American Journal of Human Genetics|March 1, 1991

Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, et al.

Experimental and Clinical Immunogenetics|January 1, 1993

Identification of a new DNA polymorphism tightly linked to DQ-alpha locusP Gasparini, A Bonizzato, A Totaro, et al.

Science (New York, N.Y.)|November 17, 2001

Seismic evidence of an extended magmatic sill under Mt. VesuviusE Auger, P Gasparini, J Virieux, et al.

Human Mutation|January 1, 1994

Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutationsL Bisceglia, A Grifa, L Zelante, et al.

Pageof 25