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Publications by Katharina Wimmer
Clinical Utility Gene Card For: Tuberous Sclerosis Complex (TSC1, TSC2)
European Journal of Human Genetics
Genetics
Seltene Tumordispositionssyndrome Mit Manifestation Im Kindesalter
Medizinische Genetik
Genetics
A Patient Severely Affected by Spinal Neurofibromas Carries a Recurrent Splice Site Mutation in the NF1 Gene
European Journal of Human Genetics
Genetics
