9 results on '"Peters, Hartmut"'
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2. Deletions of the RUNX2 Gene Are Present in About 10% of Individuals with Cleidocranial Dysplasia
3. A New Autosomal Recessive Syndrome Characterized by Ocular Hypertelorism, Distinctive Face, Mental Retardation, Brachydactyly, and Genital Abnormalities
4. Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation
5. Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
6. Hay-Wells syndrome in a child with mutation in the TP73L gene
7. Hay-Wells syndrome in a child with mutation in the TP73L gene
8. Mutation analysis of BRCA1 and BRCA2 genes in Iranian high risk breast cancer families
9. Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification
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