Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Nafa

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Human Molecular Genetics|January 1, 1993
G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favismK Nafa, A Reghis, N Osmani, et al.
Human Genetics|April 1, 1990
Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in AlgeriaK Nafa, F Meriane, A Reghis, et al.
Human Genetics|November 1, 1994
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in AlgeriaK Nafa, A Reghis, N Osmani, et al.
Blood|September 26, 2000
Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuriaA Karadimitris, J S Manavalan, H T Thaler, et al.
Cancer|June 23, 2015
Epidermal growth factor receptor exon 20 insertions in advanced lung adenocarcinomas: Clinical outcomes and response to erlotinibJ Naidoo, C S Sima, K Rodriguez, et al.
British Journal of Haematology|February 15, 2002
Association of clonal T-cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): further evidence for a pathogenetic link between T cells, aplastic anaemia and PNHA Karadimitris, K Li, R Notaro, et al.
Journal of Medical Genetics|August 6, 2002
Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer familiesN D Kauff, P Perez-Segura, M E Robson, et al.
Cancer Research|December 3, 1999
TbetaR-I(6A) is a candidate tumor susceptibility alleleB Pasche, P Kolachana, K Nafa, et al.
British Journal of Haematology|November 13, 2001
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuriaD J Araten, D Swirsky, A Karadimitris, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Mendelian diseases among Roman Jews: implications for the origins of disease allelesC Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|January 1, 1993
G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favismK Nafa, A Reghis, N Osmani, et al.
Human Genetics|April 1, 1990
Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in AlgeriaK Nafa, F Meriane, A Reghis, et al.
Human Genetics|November 1, 1994
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in AlgeriaK Nafa, A Reghis, N Osmani, et al.
Blood|September 26, 2000
Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuriaA Karadimitris, J S Manavalan, H T Thaler, et al.
Cancer|June 23, 2015
Epidermal growth factor receptor exon 20 insertions in advanced lung adenocarcinomas: Clinical outcomes and response to erlotinibJ Naidoo, C S Sima, K Rodriguez, et al.
British Journal of Haematology|February 15, 2002
Association of clonal T-cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): further evidence for a pathogenetic link between T cells, aplastic anaemia and PNHA Karadimitris, K Li, R Notaro, et al.
Journal of Medical Genetics|August 6, 2002
Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer familiesN D Kauff, P Perez-Segura, M E Robson, et al.
Cancer Research|December 3, 1999
TbetaR-I(6A) is a candidate tumor susceptibility alleleB Pasche, P Kolachana, K Nafa, et al.
British Journal of Haematology|November 13, 2001
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuriaD J Araten, D Swirsky, A Karadimitris, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Mendelian diseases among Roman Jews: implications for the origins of disease allelesC Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Pageof 3