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Nederlands Tijdschrift Voor Geneeskunde|January 22, 2026
[A man with axillary and inguinal freckling, café-au-lait spots, and cutaneous nodules]Minke J Peeters, Marjoleine F Broekema, Inge B Mathijssen
Nederlands Tijdschrift Voor Geneeskunde|July 28, 2022
[A female with excessive wrinkling of the hands]Jonathan W J Melger, Patricia J C Knijnenburg, Inge B Mathijssen
European Journal of Medical Genetics|March 15, 2006
Testicular cancer in a patient with Primrose syndromeInge B Mathijssen, Jos van Hasselt-van der Velde, Raoul C M Hennekam
European Journal of Human Genetics : EJHG|August 11, 2020
How will new genetic technologies, such as gene editing, change reproductive decision-making? Views of high-risk couplesIvy van Dijke, Phillis Lakeman, Inge B Mathijssen, et al.
Molecular Cytogenetics|January 31, 2012
Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicismKarin Huijsdens-van Amsterdam, Daniela Qcm Barge-Schaapveld, Inge B Mathijssen, et al.
European Journal of Public Health|August 4, 2016
Factors for successful implementation of population-based expanded carrier screening: learning from existing initiativesKim C A Holtkamp, Inge B Mathijssen, Phillis Lakeman, et al.
European Journal of Human Genetics : EJHG|June 22, 2021
Couples' experiences with expanded carrier screening: evaluation of a university hospital screening offerIvy van Dijke, Phillis Lakeman, Naoual Sabiri, et al.
Journal of Clinical Lipidology|January 5, 2023
Counseling couples at risk of having a child with homozygous familial hypercholesterolemia - Clinical experience and recommendationsTycho R Tromp, M Doortje Reijman, Albert Wiegman, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Homozygous DMRT2 variant associates with severe rib malformations in a newbornArjan Bouman, Quinten Waisfisz, Jop Admiraal, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndromeInge B Mathijssen, Jan M N Hoovers, Adri N P M Mul, et al.
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