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

F Bernini

Showing results (151-160 of 172) with videos related to

Pageof 18
Sort By:
British Journal of Haematology|November 25, 1998
A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutationP C Giordano, C L Harteveld, H L Haak, et al.
Human Genetics|June 30, 1977
Localization of HLA on the short arm of chromosome 6M H Breuning, E M van den Berg-Loonen, L F Bernini, et al.
British Journal of Haematology|December 1, 1996
An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch familiesC L Harteveld, J G Heister, P C Giordano, et al.
British Journal of Haematology|December 1, 1986
ABO and Rhesus phenotyping of fetal erythrocytes in the first trimester of pregnancyR J Gemke, H H Kanhai, M A Overbeeke, et al.
American Journal of Human Genetics|March 20, 2001
An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populationsM Kayser, M Krawczak, L Excoffier, et al.
Human Genetics|January 1, 1984
Genetic linkage between erythrokeratodermia variabilis and Rh locusJ G van der Schroeff, L E Nijenhuis, P Meera Khan, et al.
Prenatal Diagnosis|December 17, 1998
Two-colour immunocytochemical staining of gamma (gamma) and epsilon (epsilon) type haemoglobin in fetal red cellsW E Mesker, M C Ouwerkerk-van Velzen, J C Oosterwijk, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|April 1, 2014
Flow-mediated dilation, carotid wall thickness and HDL function in subjects with hyperalphalipoproteinemiaG B Vigna, E Satta, F Bernini, et al.
Hemoglobin|May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 1, 1996
Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene productD J Peters, L Spruit, R Klingel, et al.
Pageof 18

Showing results (151-160 of 172) with videos related to

Sort By:
Pageof 18
British Journal of Haematology|November 25, 1998
A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutationP C Giordano, C L Harteveld, H L Haak, et al.
Human Genetics|June 30, 1977
Localization of HLA on the short arm of chromosome 6M H Breuning, E M van den Berg-Loonen, L F Bernini, et al.
British Journal of Haematology|December 1, 1996
An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch familiesC L Harteveld, J G Heister, P C Giordano, et al.
British Journal of Haematology|December 1, 1986
ABO and Rhesus phenotyping of fetal erythrocytes in the first trimester of pregnancyR J Gemke, H H Kanhai, M A Overbeeke, et al.
American Journal of Human Genetics|March 20, 2001
An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populationsM Kayser, M Krawczak, L Excoffier, et al.
Human Genetics|January 1, 1984
Genetic linkage between erythrokeratodermia variabilis and Rh locusJ G van der Schroeff, L E Nijenhuis, P Meera Khan, et al.
Prenatal Diagnosis|December 17, 1998
Two-colour immunocytochemical staining of gamma (gamma) and epsilon (epsilon) type haemoglobin in fetal red cellsW E Mesker, M C Ouwerkerk-van Velzen, J C Oosterwijk, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|April 1, 2014
Flow-mediated dilation, carotid wall thickness and HDL function in subjects with hyperalphalipoproteinemiaG B Vigna, E Satta, F Bernini, et al.
Hemoglobin|May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 1, 1996
Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene productD J Peters, L Spruit, R Klingel, et al.
Pageof 18