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Wijsman

Showing results (281-290 of 511) with videos related to

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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|January 27, 2023
Inter- and intrafractional 4D dose accumulation for evaluating ΔNTCP robustness in lung cancerAndreas Smolders, Adriaan C Hengeveld, Stefan Both, et al.
Frontiers in Psychology|October 10, 2022
Validity and reliability of the Musicians' Health Literacy Questionnaire, MHL-Q19Christine Guptill, Teri Slade, Vera Baadjou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15qNicola H Chapman, Robert P Igo, Jennifer B Thomson, et al.
Annals of Neurology|June 18, 1998
Tau is a candidate gene for chromosome 17 frontotemporal dementiaP Poorkaj, T D Bird, E Wijsman, et al.
Genomics|October 1, 1994
Homozygosity mapping of the Werner syndrome locus (WRN)J Nakura, E M Wijsman, T Miki, et al.
Computers in Biology and Medicine|May 31, 2024
Probability maps for deep learning-based head and neck tumor segmentation: Graphical User Interface design and testAlessia De Biase, Liv Ziegfeld, Nanna Maria Sijtsema, et al.
Neurology|April 1, 1997
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FADT D Bird, E M Wijsman, D Nochlin, et al.
BMJ Simulation & Technology Enhanced Learning|May 6, 2022
Comparison of the psychological and physiological effects on students of a video-assisted or text introduction to a simulated taskAnne Ac van Tetering, Jacqueline Lp Wijsman, Sophie Em Truijens, et al.
American Journal of Human Genetics|November 26, 2013
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemiaElisabeth A Rosenthal, Jane Ranchalis, David R Crosslin, et al.
Human Genetics|October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorderN H Chapman, R A Bernier, S J Webb, et al.
Pageof 52

Showing results (281-290 of 511) with videos related to

Sort By:
Pageof 52
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|January 27, 2023
Inter- and intrafractional 4D dose accumulation for evaluating ΔNTCP robustness in lung cancerAndreas Smolders, Adriaan C Hengeveld, Stefan Both, et al.
Frontiers in Psychology|October 10, 2022
Validity and reliability of the Musicians' Health Literacy Questionnaire, MHL-Q19Christine Guptill, Teri Slade, Vera Baadjou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15qNicola H Chapman, Robert P Igo, Jennifer B Thomson, et al.
Annals of Neurology|June 18, 1998
Tau is a candidate gene for chromosome 17 frontotemporal dementiaP Poorkaj, T D Bird, E Wijsman, et al.
Genomics|October 1, 1994
Homozygosity mapping of the Werner syndrome locus (WRN)J Nakura, E M Wijsman, T Miki, et al.
Computers in Biology and Medicine|May 31, 2024
Probability maps for deep learning-based head and neck tumor segmentation: Graphical User Interface design and testAlessia De Biase, Liv Ziegfeld, Nanna Maria Sijtsema, et al.
Neurology|April 1, 1997
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FADT D Bird, E M Wijsman, D Nochlin, et al.
BMJ Simulation & Technology Enhanced Learning|May 6, 2022
Comparison of the psychological and physiological effects on students of a video-assisted or text introduction to a simulated taskAnne Ac van Tetering, Jacqueline Lp Wijsman, Sophie Em Truijens, et al.
American Journal of Human Genetics|November 26, 2013
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemiaElisabeth A Rosenthal, Jane Ranchalis, David R Crosslin, et al.
Human Genetics|October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorderN H Chapman, R A Bernier, S J Webb, et al.
Pageof 52