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Journal of Molecular Medicine (Berlin, Germany)|March 25, 2014
Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testingThomas Eggermann, Ann-Kathrin Heilsberg, Susanne Bens, et al.
Clinical Epigenetics|October 20, 2017
Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challengeSusanne Bens, Manuel Luedeke, Tanja Richter, et al.
Free Neuropathology|June 7, 2023
Desmoplastic myxoid tumor of pineal region, SMARCB1-mutant, in young adultBranavan Manoranjan, Yves P Starreveld, Robert A Nordal, et al.
Fertility and Sterility|February 15, 2014
Array-based DNA methylation profiling in male infertility reveals allele-specific DNA methylation in PIWIL1 and PIWIL2Carolin Friemel, Ole Ammerpohl, Jana Gutwein, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysisTill Holsten, Susanne Bens, Florian Oyen, et al.
Journal of Neuropathology and Experimental Neurology|March 14, 2013
Mechanisms of intracerebral lymphoma growth delineated in a syngeneic mouse model of central nervous system lymphomaManuel Montesinos-Rongen, Mónica Sánchez-Ruiz, Anna Brunn, et al.
Molecular and Cellular Pediatrics|August 12, 2016
Transient spontaneous remission in congenital MLL-AF10 rearranged acute myeloid leukemia presenting with cardiorespiratory failure and meconium ileusTobias Gyárfás, Juergen Wintgens, Wolfgang Biskup, et al.
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