5 results on '"Oexle Konrad"'
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2. Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion
3. Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation
4. Reply to “Should a syndrome be called by its correct name? The example of the preserved speech variant of Rett syndrome” by Zappella et al.
5. Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion
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