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bibliographicCitation Jülich K, Horn D, Burfeind P, Erler T, Auber B. A Novel MECP2 Mutation in a Boy with Neonatal Encephalopathy and Facial Dysmorphism. The Journal of Pediatrics. 2009 Jul;155(1):140–3. doi: 10.1016/j.jpeds.2009.01.035.
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title A Novel MECP2 Mutation in a Boy with Neonatal Encephalopathy and Facial Dysmorphism
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