Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy
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J. Gécz | A. Green | B. Echenne | H. Bokhoven | T. Kleefstra | B. Hamel | D. Lacombe | A. Tzschach | J. Chelly | J. Pedespan | A. Brouwer | H. Esch | M. Raynaud | M. King | D. Rating | C. Goizet | D. Lugtenberg | H. Yntema | W. Nillesen | A. Oudakker | H. Journel | D. O'Rourke | G. Tariverdian | M. Kogelenberg | Astrid R. Oudakker
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