Marc Sylva
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making.
Journal: European journal of human genetics : EJHG
Published: March 24, 2025
Severe Fetal Hemolysis and Cholestasis Due to High-Titer Maternal IgG Anti-A Antibodies.
Journal: Pediatrics
Published: November 15, 2018
Identifying pathogenic variants in the Follistatin-like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disorders.
Journal: Molecular genetics & genomic medicine
Published: November 13, 2018
Deletion of Fstl1 (Follistatin-Like 1) From the Endocardial/Endothelial Lineage Causes Mitral Valve Disease.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: January 23, 2017
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal.
Journal: Journal of medical genetics
Published: November 21, 2013
Follistatin-like 1 in vertebrate development.
Journal: Birth defects research. Part C, Embryo today : reviews
Published: January 23, 2013
Development of the human heart.
Journal: American journal of medical genetics. Part A
Published: August 07, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026