Janneke Schuurs-Hoeijmakers
- Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
2015/07/30 by Lot Snijders Blok, Lot Snijders Blok, Erik Madsen +123 · 30 citations
Biochemistry, Genetics and Molecular Biology · #Genetics and Neurodevelopmental Disorders #Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities #Congenital heart defects research
- Presence of Genetic Variants Among Young Men With Severe COVID-19
2020/07/24 by Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers +27 · 4 citations
Immunology and Microbiology · #Complement system in diseases #Immune responses and vaccinations #Immunodeficiency and Autoimmune Disorders