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Publications by Isabelle Schrauwen

Delineating the GRIN1 Phenotypic Spectrum

English

Genome-Wide Analysis Reveals a Novel Autosomal-Recessive Hearing Loss Locus DFNB80 on Chromosome 2p16.1-P21

Journal of Human Genetics

English

Advances in Molecular Genetics and the Molecular Biology of Deafness

BioMed Research International

Molecular Biology

English

A Start Codon Variant in NOG Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes

Case Reports in Genetics

English

A Genome-Wide Analysis Identifies Genetic Variants in the RELN Gene Associated With Otosclerosis

American Journal of Human Genetics

English

Association of Bone Morphogenetic Proteins With Otosclerosis

Journal of Bone and Mineral Research

Sports Medicine

English