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European Journal of Human Genetics : EJHG|December 20, 2007
Provision and quality assurance of preimplantation genetic diagnosis in EuropeAnniek Corveleyn, Michael A Morris, Elisabeth Dequeker, et al.Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experienceChristine Van Laer, Marc Jacquemin, Sarissa Baert, et al.European Journal of Human Genetics : EJHG|April 9, 2023
Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRIJohanna Jacobs, Lucas Van Aelst, Jeroen Breckpot, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 16, 2014
Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tractAnke Raaijmakers, Anniek Corveleyn, Koen Devriendt, et al.Plos Genetics|January 23, 2018
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblingsJacoba J Louw, Ricardo Nunes Bastos, Xiaowen Chen, et al.American Journal of Medical Genetics. Part A|May 2, 2015
The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defectsYaojuan Jia, Jacoba J Louw, Jeroen Breckpot, et al.Frontiers in Immunology|November 2, 2020
Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the LiteratureFrederik Staels, Albrecht Betrains, Peter Doubel, et al.European Journal of Human Genetics : EJHG|October 29, 2015
Guidelines for diagnostic next-generation sequencingGert Matthijs, Erika Souche, Mariëlle Alders, et al.Clinical Immunology (Orlando, Fla.)|March 1, 2026
Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial diseaseWillem Roosens, Marjon Wouters, Frederik Staels, et al.American Journal of Medical Genetics. Part A|August 9, 2018
A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR CongoAimé Lumaka, Valerie Race, Hilde Peeters, et al.Pageof 5