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P Fortina

Showing results (11-20 of 67) with videos related to

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The Journal of Pediatrics|September 17, 1998
Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorderG A Meyer, N J Blum, W Hitchcock, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Parallel molecular genetic analysisS E McKenzie, E Mansfield, E Rappaport, et al.
American Journal of Hematology|October 1, 1996
Human alpha-thalassemia syndromes: detection of molecular defectsA C Kattamis, C Camaschella, P Sivera, et al.
Annals of Clinical Biochemistry|November 30, 2006
Current perspectives in protein array technologyLarry J Kricka, S R Master, T O Joos, et al.
Minerva Ginecologica|June 1, 1986
[Early recognition of twin-to-twin transfusion syndrome. Differential diagnosis and therapeutic hypothesis]M Campogrande, A La Prova, G Cornaglia, et al.
Biotechniques|February 19, 2002
Four-laser scanning confocal system for microarray analysisD J Graves, H J Su, S Addya, et al.
Analytical Chemistry|December 16, 1998
System for preparing microhybridization arrays on glass slidesD J Graves, H J Su, S E McKenzie, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Indian Journal of Human Genetics|March 20, 2010
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridizationM Chetta, A Drmanac, R Santacroce, et al.
Progress in Clinical and Biological Research|January 1, 1989
Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humansP Fortina, K Delgrosso, E Rappaport, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
The Journal of Pediatrics|September 17, 1998
Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorderG A Meyer, N J Blum, W Hitchcock, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Parallel molecular genetic analysisS E McKenzie, E Mansfield, E Rappaport, et al.
American Journal of Hematology|October 1, 1996
Human alpha-thalassemia syndromes: detection of molecular defectsA C Kattamis, C Camaschella, P Sivera, et al.
Annals of Clinical Biochemistry|November 30, 2006
Current perspectives in protein array technologyLarry J Kricka, S R Master, T O Joos, et al.
Minerva Ginecologica|June 1, 1986
[Early recognition of twin-to-twin transfusion syndrome. Differential diagnosis and therapeutic hypothesis]M Campogrande, A La Prova, G Cornaglia, et al.
Biotechniques|February 19, 2002
Four-laser scanning confocal system for microarray analysisD J Graves, H J Su, S Addya, et al.
Analytical Chemistry|December 16, 1998
System for preparing microhybridization arrays on glass slidesD J Graves, H J Su, S E McKenzie, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Indian Journal of Human Genetics|March 20, 2010
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridizationM Chetta, A Drmanac, R Santacroce, et al.
Progress in Clinical and Biological Research|January 1, 1989
Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humansP Fortina, K Delgrosso, E Rappaport, et al.
Pageof 7