Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Human Mutation|June 24, 2008
Somatic mosaicism for copy number variation in differentiated human tissuesArkadiusz Piotrowski, Carl E G Bruder, Robin Andersson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2020
Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfallsKevin M Bowling, Michelle L Thompson, David E Gray, et al.
HGG Advances|May 3, 2021
Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
European Journal of Human Genetics : EJHG|January 7, 2010
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progressionAndrzej B Popławski, Michał Jankowski, Stephen W Erickson, et al.
Nature|July 31, 2020
Occupancy maps of 208 chromatin-associated proteins in one human cell typeE Christopher Partridge, Surya B Chhetri, Jeremy W Prokop, et al.
American Journal of Human Genetics|February 29, 2008
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profilesCarl E G Bruder, Arkadiusz Piotrowski, Antoinet A C J Gijsbers, et al.
Oncotarget|December 29, 2016
Genomic regulation of invasion by STAT3 in triple negative breast cancerJoy M McDaniel, Katherine E Varley, Jason Gertz, et al.
American Journal of Physiology. Cell Physiology|July 25, 2025
Methyl-CpG-binding domain as a protein interaction partner in promoter regulation and neurodevelopment through evolutionary expanded entanglementStephanie M Bilinovich, Surya B Chhetri, Jackson T Mitchell, et al.
Nature|September 8, 2012
Architecture of the human regulatory network derived from ENCODE dataMark B Gerstein, Anshul Kundaje, Manoj Hariharan, et al.
American Journal of Human Genetics|December 31, 2022
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotypeSusan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, et al.
Pageof 2