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L F Bernini

Showing results (61-70 of 73) with videos related to

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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.
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.
Human Genetics|January 1, 1984
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch familyF H Menko, O L Bijvoet, P Meera Khan, et al.
Annals of Hematology|January 6, 1999
Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G-->T) mutationP C Giordano, C L Harteveld, J J Michiels, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
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.
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.
Human Genetics|January 1, 1984
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch familyF H Menko, O L Bijvoet, P Meera Khan, et al.
Annals of Hematology|January 6, 1999
Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G-->T) mutationP C Giordano, C L Harteveld, J J Michiels, et al.
Pageof 8