5 results on '"Peters, Hartmut"'
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2. A novel mutation L1425p in the GAP-region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE);
3. Mutation screening of neurofibromatosis type 1 (NF1) exons 28 and 29 with single strand conformation polymorphism (SSCP): Five novel mutations, one recurrent transition and two polymorphisms in a panel of 118 unrelated NF1 patients
4. A novel 5-bp deletion in exon 30 of the neurofibromatosis type 1 (NF1) gene
5. A rapid screening for steroid 21-hydroxylase mutations in patients with congenital adrenal hyperplasia
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