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Publications by Sabine Lüttgen

Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation

Genetics in Medicine
MedicineGenetics
2016English

Novel Mutations in BCOR in Three Patients With Oculo-Facio-Cardio-Dental Syndrome, but None in Lenz Microphthalmia Syndrome

European Journal of Human Genetics
Genetics
2005English

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