Human Genome Epidemiology Literature Finder
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Query Trace: Fragile X Syndrome and MECP2[original query] |
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MECP2 mutation analysis in patients with mental retardation. American journal of medical genetics. Part A 2005 Jan 132A (2): 121-4. Ylisaukko-Oja Tero, Rehnström Karola, Vanhala Raija, Kempas Elli, von Koskull Harriet, Tengström Carola, Mustonen Aki, Ounap Katrin, Lähdetie Jaana, Järvelä Ir |
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