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Showing results (1301-1310 of 1,358) with videos related to

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Human Molecular Genetics|October 12, 2014
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisMariana Ramos-Brossier, Caterina Montani, Nicolas Lebrun, et al.
Blood|February 7, 2001
A 2-step comprehensive high-dose chemoradiotherapy second-line program for relapsed and refractory Hodgkin disease: analysis by intent to treat and development of a prognostic modelC H Moskowitz, S D Nimer, A D Zelenetz, et al.
Clinical Epigenetics|January 9, 2020
Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signatureAndrea Ciolfi, Erfan Aref-Eshghi, Simone Pizzi, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approachesDavid A Koolen, Erik A Sistermans, Willy Nilessen, et al.
Scientific Reports|June 26, 2024
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patientsClaudio Peter D'Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 30, 1999
Ifosfamide, carboplatin, and etoposide: a highly effective cytoreduction and peripheral-blood progenitor-cell mobilization regimen for transplant-eligible patients with non-Hodgkin's lymphomaC H Moskowitz, J R Bertino, J R Glassman, et al.
Medical Teacher|July 29, 2010
Competency-based medical education: theory to practiceJason R Frank, Linda S Snell, Olle Ten Cate, et al.
Biological Psychiatry|May 5, 2018
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNPAnke Van Dijck, Anneke T Vulto-van Silfhout, Elisa Cappuyns, et al.
Nature Genetics|August 15, 2006
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphismDavid A Koolen, Lisenka E L M Vissers, Rolph Pfundt, et al.
Journal of Medical Genetics|April 15, 2016
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotypeGea Beunders, Jiddeke van de Kamp, Pradeep Vasudevan, et al.
Pageof 136

Showing results (1301-1310 of 1,358) with videos related to

Sort By:
Pageof 136
Human Molecular Genetics|October 12, 2014
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisMariana Ramos-Brossier, Caterina Montani, Nicolas Lebrun, et al.
Blood|February 7, 2001
A 2-step comprehensive high-dose chemoradiotherapy second-line program for relapsed and refractory Hodgkin disease: analysis by intent to treat and development of a prognostic modelC H Moskowitz, S D Nimer, A D Zelenetz, et al.
Clinical Epigenetics|January 9, 2020
Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signatureAndrea Ciolfi, Erfan Aref-Eshghi, Simone Pizzi, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approachesDavid A Koolen, Erik A Sistermans, Willy Nilessen, et al.
Scientific Reports|June 26, 2024
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patientsClaudio Peter D'Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 30, 1999
Ifosfamide, carboplatin, and etoposide: a highly effective cytoreduction and peripheral-blood progenitor-cell mobilization regimen for transplant-eligible patients with non-Hodgkin's lymphomaC H Moskowitz, J R Bertino, J R Glassman, et al.
Medical Teacher|July 29, 2010
Competency-based medical education: theory to practiceJason R Frank, Linda S Snell, Olle Ten Cate, et al.
Biological Psychiatry|May 5, 2018
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNPAnke Van Dijck, Anneke T Vulto-van Silfhout, Elisa Cappuyns, et al.
Nature Genetics|August 15, 2006
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphismDavid A Koolen, Lisenka E L M Vissers, Rolph Pfundt, et al.
Journal of Medical Genetics|April 15, 2016
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotypeGea Beunders, Jiddeke van de Kamp, Pradeep Vasudevan, et al.
Pageof 136