Human Genome Epidemiology Literature Finder
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Query Trace: Atrophy and MECP2[original query] |
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Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy. European journal of human genetics : EJHG 2009 Apr 17 (4): 444-53. Lugtenberg Dorien, Kleefstra Tjitske, Oudakker Astrid R, Nillesen Willy M, Yntema Helger G, Tzschach Andreas, Raynaud Martine, Rating Dietz, Journel Hubert, Chelly Jamel, Goizet Cyril, Lacombe Didier, Pedespan Jean-Michel, Echenne Bernard, Tariverdian Gholamali, O'Rourke Declan, King Mary D, Green Andrew, van Kogelenberg Margriet, Van Esch Hilde, Gecz Jozef, Hamel Ben C J, van Bokhoven Hans, de Brouwer Arjan P |
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