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Journal of Medical Genetics|October 24, 2007
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyA I Jonckheere, M Hogeveen, L G J Nijtmans, et al.
Nature Genetics|August 10, 2004
Mutations in a new member of the chromodomain gene family cause CHARGE syndromeLisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, et al.
Bioconjugate Chemistry|March 21, 2017
Investigating the Cellular Specificity in Tumors of a Surface-Converting Nanoparticle by Multimodal ImagingFrancois Fay, Line Hansen, Stefanie J C G Hectors, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|January 13, 2024
Exploring the interconnectedness between health-related quality of life factors among long-term adolescent and young adult cancer survivors (AYAs): a network analysisTom I Bootsma, Deborah van de Wal, Carla Vlooswijk, et al.
Blood|April 20, 2018
RNA-based FLT3-ITD allelic ratio is associated with outcome and ex vivo response to FLT3 inhibitors in pediatric AMLDavid G J Cucchi, Barbara Denys, Gertjan J L Kaspers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 3, 2017
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disordersRolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, et al.
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