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Publications by Koen Devriendt
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
American Journal of Human Genetics
Genetics
Defective DNA Polymerase Α-Primase Leads to X-Linked Intellectual Disability Associated With Severe Growth Retardation, Microcephaly, and Hypogonadism
American Journal of Human Genetics
Genetics
Expanding the Clinical and Mutational Spectrum of the Ehlers–Danlos Syndrome, Dermatosparaxis Type
Genetics in Medicine
Medicine
Genetics
Pseudoautosomal Region 1 Length Polymorphism in the Human Population
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Platelet Defects in Congenital Variant of Rett Syndrome Patients With FOXG1 Mutations or Reduced Expression Due to a Position Effect at 14q12
European Journal of Human Genetics
Genetics
Novel Mutation in the Per-Arnt-Sim Domain of KCNH2 Causes a Malignant Form of Long-Qt Syndrome
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
American Journal of Human Genetics
Genetics
Identification and Characterization of the TRIP8 and REEP3 Genes on Chromosome 10q21.3 as Novel Candidate Genes for Autism
European Journal of Human Genetics
Genetics
