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Molecular Syndromology|October 30, 2010
Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1AR Oegema, A de Klein, A J Verkerk, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 14, 2017
Monocytes and Granulocytes Reduce CD38 Expression Levels on Myeloma Cells in Patients Treated with DaratumumabJakub Krejcik, Kris A Frerichs, Inger S Nijhof, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalusAnnemieke J M H Verkerk, Rachel Schot, Laura van Waterschoot, et al.
Elife|January 18, 2021
Loss of FLCN-FNIP1/2 induces a non-canonical interferon response in human renal tubular epithelial cellsIris E Glykofridis, Jaco C Knol, Jesper A Balk, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Nature Genetics|November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomaliesClaire Redin, Harrison Brand, Ryan L Collins, et al.
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