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Journal of Medical Genetics|October 27, 2012
Risk of malignant paraganglioma in SDHB-mutation and SDHD-mutation carriers: a systematic review and meta-analysisLeonie Theresia van Hulsteijn, Olaf M Dekkers, Frederik J Hes, et al.
World Journal of Surgical Oncology|October 23, 2012
Case of spontaneous regression of carotid body tumor in a SDHD mutant: a discussion on potential mechanisms based on a review of the literatureSebastiaan Hammer, Jeroen C Jansen, Eleonora P M van der Kleij-Corssmit, et al.
The Journal of Clinical Endocrinology and Metabolism|February 28, 2024
Clinically Relevant Germline Variants in Children With Nonmedullary Thyroid CancerKarin van der Tuin, Dina Ruano, Jeroen Knijnenburg, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
No evidence for increased mortality in SDHD variant carriers compared with the general populationLeonie T van Hulsteijn, Berdine Heesterman, Jeroen C Jansen, et al.
F&S Reports|October 7, 2025
Do children born after embryo vitrification differ from siblings born after fresh embryo transfer?Florence Belva, Christophe Blockeel, Mathieu Roelants, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 3, 2015
[CHEK2-mutation in Dutch breast cancer families: expanding genetic testing for breast cancer]Muriel A Adank, Frederik J Hes, Wendy A G van Zelst-Stams, et al.
European Journal of Human Genetics : EJHG|June 15, 2007
Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature reviewMaartje Nielsen, Elsa Bik, Frederik J Hes, et al.
Familial Cancer|July 23, 2014
Phenotype of SDHB mutation carriers in the NetherlandsLeonie T van Hulsteijn, Nienke D Niemeijer, Frederik J Hes, et al.
Molecular Genetics & Genomic Medicine|March 4, 2019
Low frequency of POLD1 and POLE exonuclease domain variants in patients with multiple colorectal polypsFadwa A Elsayed, Carli M J Tops, Maartje Nielsen, et al.
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