Showing results (271-280 of 311) with videos related to

Sort By:
Pageof 32
Human Mutation|September 10, 2019
Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculatureChantal Kerkhofs, Servi J C Stevens, Saul N Faust, et al.
The Pediatric Infectious Disease Journal|January 1, 1997
Sequential ciprofloxacin therapy in pediatric cystic fibrosis: comparative study vs. ceftazidime/tobramycin in the treatment of acute pulmonary exacerbations. The Cystic Fibrosis Study GroupD A Church, J F Kanga, R J Kuhn, et al.
American Journal of Medical Genetics. Part A|September 24, 2025
Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16BServi J C Stevens, Wanwisa van Dijk, Nicole Y Souren, et al.
Human Mutation|April 25, 2018
De novo mutations in the SET nuclear proto-oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disabilityServi J C Stevens, Vyne van der Schoot, Magalie S Leduc, et al.
Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocationsChris M J van Uum, Servi J C Stevens, Joseph C F M Dreesen, et al.
Human Reproduction (Oxford, England)|September 23, 2022
Embryo tracking system for high-throughput sequencing-based preimplantation genetic testingWanwisa van Dijk, Kasper Derks, Marion Drüsedau, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 16, 2013
Epstein-Barr virus DNA load in nasopharyngeal brushings and whole blood in nasopharyngeal carcinoma patients before and after treatmentMarlinda Adham, Astrid E Greijer, Sandra A W M Verkuijlen, et al.
Genome Medicine|December 15, 2016
Truncating de novo mutations in the Krüppel-type zinc-finger gene ZNF148 in patients with corpus callosum defects, developmental delay, short stature, and dysmorphismsServi J C Stevens, Anthonie J van Essen, Conny M A van Ravenswaaij, et al.
American Journal of Medical Genetics. Part A|October 13, 2011
MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletionsServi J C Stevens, Conny M A van Ravenswaaij-Arts, Jannie W H Janssen, et al.
Pageof 32