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Marianne Stef

Showing results (1-10 of 20) with videos related to

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Transfusion|May 14, 2026
A serologic weak D expressed by a combined weak D type 1/41.0.1 alleleDonatella Londero, Chiara Sindici, Marianne Stef, et al.
Transfusion|March 7, 2025
JK*01(307C) encodes a JK null alleleVonya Drinnon, Amanda Graves, Cres Levin, et al.
Biochimica Et Biophysica Acta|May 26, 2005
Profiling candidate genes involved in wax biosynthesis in Arabidopsis thaliana by microarray analysisPatricia Costaglioli, Jérôme Joubès, Christel Garcia, et al.
Atherosclerosis|January 17, 2012
Molecular characterization of familial hypercholesterolemia in SpainLourdes Palacios, Laura Grandoso, Nerea Cuevas, et al.
Transfusion|September 2, 2020
RH genotyping by nonspecific quantitative next-generation sequencingMarianne Stef, Katie Fennell, Izaskun Apraiz, et al.
European Journal of Medical Genetics|November 21, 2007
A 580 kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformationCaroline Rooryck, Ingrid Burgelin, Marianne Stef, et al.
Human Mutation|November 8, 2014
Functional characterization and classification of frequent low-density lipoprotein receptor variantsAitor Etxebarria, Asier Benito-Vicente, Lourdes Palacios, et al.
Human Mutation|September 5, 2006
Testing and improving experimental parameters for the use of low molecular weight targets in array-CGH experimentsMarianne Stef, Delphine Simon, Ingrid Burgelin, et al.
European Journal of Medical Genetics|September 8, 2009
2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate geneCaroline Rooryck, Marianne Stef, Ingrid Burgelin, et al.
Transfusion Medicine (Oxford, England)|July 3, 2026
First identification and molecular characterisation of a rare D- - donor in Saudi ArabiaMaymoon M Madkhali, Abdullah A Meshi, Mahdi Osman, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Transfusion|May 14, 2026
A serologic weak D expressed by a combined weak D type 1/41.0.1 alleleDonatella Londero, Chiara Sindici, Marianne Stef, et al.
Transfusion|March 7, 2025
JK*01(307C) encodes a JK null alleleVonya Drinnon, Amanda Graves, Cres Levin, et al.
Biochimica Et Biophysica Acta|May 26, 2005
Profiling candidate genes involved in wax biosynthesis in Arabidopsis thaliana by microarray analysisPatricia Costaglioli, Jérôme Joubès, Christel Garcia, et al.
Atherosclerosis|January 17, 2012
Molecular characterization of familial hypercholesterolemia in SpainLourdes Palacios, Laura Grandoso, Nerea Cuevas, et al.
Transfusion|September 2, 2020
RH genotyping by nonspecific quantitative next-generation sequencingMarianne Stef, Katie Fennell, Izaskun Apraiz, et al.
European Journal of Medical Genetics|November 21, 2007
A 580 kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformationCaroline Rooryck, Ingrid Burgelin, Marianne Stef, et al.
Human Mutation|November 8, 2014
Functional characterization and classification of frequent low-density lipoprotein receptor variantsAitor Etxebarria, Asier Benito-Vicente, Lourdes Palacios, et al.
Human Mutation|September 5, 2006
Testing and improving experimental parameters for the use of low molecular weight targets in array-CGH experimentsMarianne Stef, Delphine Simon, Ingrid Burgelin, et al.
European Journal of Medical Genetics|September 8, 2009
2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate geneCaroline Rooryck, Marianne Stef, Ingrid Burgelin, et al.
Transfusion Medicine (Oxford, England)|July 3, 2026
First identification and molecular characterisation of a rare D- - donor in Saudi ArabiaMaymoon M Madkhali, Abdullah A Meshi, Mahdi Osman, et al.
Pageof 2