5 results on '"Peters, Hartmut"'
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2. A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalities
3. Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation
4. Craniosynostosis in cherubism
5. Two independent mutations in a family with neurofibromatosis type 1 (NF1)
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