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Egbert Bakker

Showing results (1-10 of 52) with videos related to

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International Journal of Environmental Research and Public Health|June 13, 2014
Genetic epidemiology and preventive healthcare in multiethnic societies: the hemoglobinopathiesPiero C Giordano, Cornelis L Harteveld, Egbert Bakker
Personalized Medicine|May 17, 2018
Toward health technology assessment of whole-genome sequencing diagnostic tests: challenges and solutionsKatherine Payne, Martin Eden, Niall Davison, et al.
Neurology|December 29, 2005
Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophyEdo M Hoogerwaard, Ieke B Ginjaar, Egbert Bakker, et al.
Hemoglobin|November 6, 2014
Molecular spectrum of α-globin gene defects in the Omani populationSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.
Hemoglobin|July 3, 2014
Known and new δ-globin gene mutations and other factors influencing Hb A2 measurement in the Omani populationSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.
Hemoglobin|February 14, 2015
Broader spectrum of β-thalassemia mutations in Oman: regional distribution and comparison with neighboring countriesSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.
Haematologica|October 13, 2004
Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patientsMajid Yavarian, Mehran Karimi, Egbert Bakker, et al.
European Journal of Human Genetics : EJHG|December 9, 2004
Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutationsGeraldine R Vink, Stefan J White, Strelicija Gabelic, et al.
Plos One|May 23, 2012
Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective studyP Roberto Bakker, Egbert Bakker, Najaf Amin, et al.
Neuromuscular Disorders : NMD|May 5, 2009
Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysisRowida Almomani, Nienke van der Stoep, Egbert Bakker, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
International Journal of Environmental Research and Public Health|June 13, 2014
Genetic epidemiology and preventive healthcare in multiethnic societies: the hemoglobinopathiesPiero C Giordano, Cornelis L Harteveld, Egbert Bakker
Personalized Medicine|May 17, 2018
Toward health technology assessment of whole-genome sequencing diagnostic tests: challenges and solutionsKatherine Payne, Martin Eden, Niall Davison, et al.
Neurology|December 29, 2005
Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophyEdo M Hoogerwaard, Ieke B Ginjaar, Egbert Bakker, et al.
Hemoglobin|November 6, 2014
Molecular spectrum of α-globin gene defects in the Omani populationSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.
Hemoglobin|July 3, 2014
Known and new δ-globin gene mutations and other factors influencing Hb A2 measurement in the Omani populationSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.
Hemoglobin|February 14, 2015
Broader spectrum of β-thalassemia mutations in Oman: regional distribution and comparison with neighboring countriesSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.
Haematologica|October 13, 2004
Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patientsMajid Yavarian, Mehran Karimi, Egbert Bakker, et al.
European Journal of Human Genetics : EJHG|December 9, 2004
Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutationsGeraldine R Vink, Stefan J White, Strelicija Gabelic, et al.
Plos One|May 23, 2012
Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective studyP Roberto Bakker, Egbert Bakker, Najaf Amin, et al.
Neuromuscular Disorders : NMD|May 5, 2009
Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysisRowida Almomani, Nienke van der Stoep, Egbert Bakker, et al.
Pageof 6