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Publications by Stefan Mundlos

Thrombocytopenia-Absent Radius Syndrome

2014English

Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal Γ Subunit

American Journal of Human Genetics
Genetics
2006English

The Fibrodysplasia Ossificans Progressiva R206H ACVR1 Mutation Activates BMP-independent Chondrogenesis and Zebrafish Embryo Ventralization

Journal of Clinical Investigation
Medicine
2009English

Evolution of a Core Gene Network for Skeletogenesis in Chordates

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2008English

Modelling Neurofibromatosis Type 1 Tibial Dysplasia and Its Treatment With Lovastatin

BMC Medicine
Medicine
2008English

A Novel R486Q Mutation in BMPR1B Resulting in Either a Brachydactyly Type C/Symphalangism-Like Phenotype or Brachydactyly Type A2

European Journal of Human Genetics
Genetics
2006English

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