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European Journal of Human Genetics : EJHG|September 27, 2018
Fetal fraction evaluation in non-invasive prenatal screening (NIPS)Matthew S Hestand, Mark Bessem, Peter van Rijn, et al.
European Journal of Medical Genetics|October 5, 2014
First steps in exploring prospective exome sequencing of consanguineous couplesMarieke Teeuw, Quinten Waisfisz, Petra J G Zwijnenburg, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 4, 2008
Identification of patients with (atypical) MUTYH-associated polyposis by KRAS2 c.34G > T prescreening followed by MUTYH hotspot analysis in formalin-fixed paraffin-embedded tissueMarjo van Puijenbroek, Maartje Nielsen, Carli M J Tops, et al.
Prenatal Diagnosis|August 5, 2021
Association between low fetal fraction in cell-free DNA testing and adverse pregnancy outcome: A systematic reviewPeter G Scheffer, Soetinah A M Wirjosoekarto, Ellis C Becking, et al.
Oncogene|March 28, 2003
Genomic profiling of gastric cancer predicts lymph node status and survivalMarjan M Weiss, Ernst J Kuipers, Cindy Postma, et al.
Annals of Neurology|July 31, 2015
Recessive ITPA mutations cause an early infantile encephalopathySietske H Kevelam, Jörgen Bierau, Ramona Salvarinova, et al.
Human Molecular Genetics|August 22, 2014
Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsiaCees B M Oudejans, Omar J Michel, Rob Janssen, et al.
Endocrine-Related Cancer|June 24, 2009
Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patientsJean-Pierre Bayley, Marjan M Weiss, Anneliese Grimbergen, et al.
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