Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Hereditary Cancer in Clinical Practice|May 12, 2016
An unusual case of Cowden syndrome associated with ganglioneuromatous polyposisSteffen Pistorius, Barbara Klink, Jessica Pablik, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
6q22.33 microdeletion in a family with intellectual disability, variable major anomalies, and behavioral abnormalitiesLuisa Mackenroth, Karl Hackmann, Anke Beyer, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
Partial deletion of GLRB and GRIA2 in a patient with intellectual disabilityKarl Hackmann, Sarah Matko, Eva-Maria Gerlach, et al.
International Journal of Molecular Sciences|May 28, 2022
Different Effects of RNAi-Mediated Downregulation or Chemical Inhibition of NAMPT in an Isogenic IDH Mutant and Wild-Type Glioma Cell ModelMaximilian Clausing, Doreen William, Matthias Preussler, et al.
Nucleic Acids Research|June 6, 2017
The contribution of homology arms to nuclease-assisted genome engineeringOliver Baker, Sarah Tsurkan, Jun Fu, et al.
BMC Cancer|November 21, 2012
Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancerKarin Kast, Teresa M Neuhann, Heike Görgens, et al.
The American Journal of Surgical Pathology|April 20, 2013
A novel germline KIT mutation (p.L576P) in a family presenting with juvenile onset of multiple gastrointestinal stromal tumors, skin hyperpigmentations, and esophageal stenosisTeresa M Neuhann, Veit Mansmann, Sabine Merkelbach-Bruse, et al.
Pageof 10