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Publications by Koenraad Devriendt

Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing

English

Repeat Genetic Testing With Targeted Capture Sequencing in Primary Arrhythmia Syndrome and Cardiomyopathy

European Journal of Human Genetics

English

Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability

European Journal of Human Genetics

English

Vestibular Dysfunction Is a Manifestation of 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A

English

A Syndromic Form of Pierre Robin Sequence Is Caused by 5q23 Deletions Encompassing FBN2 and PHAX

European Journal of Medical Genetics

English

C Identification of the Major Genetic Contributors to Tetralogy of Fallot

English