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You searched for: Author/Creator van de Laar, Ingrid M.B.H.

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1. ADAMTS19‐associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype. Issue 1 (19th May 2020)

3. Biallelic Variants in ASNA1, Encoding a Cytosolic Targeting Factor of Tail-Anchored Proteins, Cause Rapidly Progressive Pediatric Cardiomyopathy. (September 2019)

4. Blood biomarkers in patients with bicuspid aortic valve disease. Issue 3 (September 2020)

6. Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives. (1st May 2018)

7. Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification. (30th September 2022)

8. Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome. (December 2018)

9. SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy. (8th January 2019)