Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Lisbeth Tranebjærg

Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome

American Journal of Human Genetics

English

Ujevnt Om Klinisk Genetikk

Tidsskrift for den Norske Laegeforening

English

En Begejstret Tvillingeforskers Bog

Tidsskrift for den Norske Laegeforening

English

Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype

American Journal of Human Genetics

English

A De Novo Missense Mutation in a Critical Domain of the X-Linked DDP Gene Causes the Typical Deafness–dystonia–optic Atrophy Syndrome

European Journal of Human Genetics

English

Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss

Otology and Neurotology

Otorhinolaryngology

Sensory Systems

English