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European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
Pediatric Blood & Cancer|July 30, 2016
Atypical teratoid/rhabdoid tumor arising in a malignant gliomaBarbara Bozzai, Martin Hasselblatt, Eszter Turányi, et al.
BMC Medical Genetics|May 7, 2015
A novel large deletion of the ICR1 region including H19 and putative enhancer elementsHelen Fryssira, Stella Amenta, Deniz Kanber, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Pediatric Blood & Cancer|February 9, 2018
The extraordinary challenge of treating patients with congenital rhabdoid tumors-a collaborative European effortKarolina Nemes, Nathalie Clément, Denis Kachanov, et al.
Genes, Chromosomes & Cancer|April 25, 2021
Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumorChristian Thomas, Kathrin Oehl-Huber, Susanne Bens, et al.
The American Journal of Surgical Pathology|November 2, 2020
A Diagnostic Approach to the Identification of Burkitt-like Lymphoma With 11q Aberration in Aggressive B-Cell LymphomasHeike Horn, Sabrina Kalmbach, Rabea Wagener, et al.
The Journal of Clinical Endocrinology and Metabolism|January 19, 2010
Congenital lipoid adrenal hyperplasia: functional characterization of three novel mutations in the STAR geneSusanne Bens, Angelika Mohn, Bilgin Yüksel, et al.
Genes, Chromosomes & Cancer|April 29, 2016
Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3)Mariela C Coccé, Balca R Mardin, Susanne Bens, et al.
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