10 results on '"Peters, Hartmut"'
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2. Ectodermal Defects and Anal Atresia in a Child with aTP63Mutation-Expanding the Phenotypic Spectrum
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 intragenicROR2mutation
5. Hay‐Wells syndrome in a child with mutation in the TP73L gene
6. Hay‐Wells‐Syndrom bei einem Kind mit Mutation auf dem Gen TP73L
7. Trinucleotide repeat expansions in the junctophilin‐3 gene are not found in caucasian patients with a huntington's disease‐like phenotype
8. Craniosynostosis in cherubism
9. Two independent mutations in a family with neurofibromatosis type 1 (NF1)
10. Ectodermal Defects and Anal Atresia in a Child with a TP63 Mutation--Expanding the Phenotypic Spectrum.
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