Jan G. Post
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 14 publications
MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset.
Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Published: July 04, 2023
Family screening in patients with isolated bicuspid aortic valve : Restriction to those with aortic dilatation is not justified.
Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Published: July 21, 2021
Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy.
Journal: Journal of medical genetics
Published: May 30, 2019
Fate and removal of trace pollutants from an anion exchange spent brine during the recovery process of natural organic matter and salts.
Journal: Water research
Published: August 13, 2018
Pathogenic effect of a TGFBR1 mutation in a family with Loeys-Dietz syndrome.
Journal: Molecular genetics & genomic medicine
Published: August 07, 2018
Yield of family screening in patients with isolated bicuspid aortic valve in a general hospital.
Journal: International journal of cardiology
Published: June 27, 2017
Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives.
Journal: International journal of cardiology
Published: June 20, 2017
Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples.
Journal: Muscle & nerve
Published: April 14, 2015
Outcome in phospholamban R14del carriers: results of a large multicentre cohort study.
Journal: Circulation. Cardiovascular genetics
Published: June 10, 2014
Last Updated: 09/26/2026