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Yntema HG, Oudakker AR, Kleefstra T, Hamel BCJ, van Bokhoven H, Chelly J, Kalscheuer VM, Fryns JP, Raynaud M, Moizard MP, Moraine C. 2002. In-frame deletion in MECP2 causes mild nonspecific mental retardation. Am J Med Genet 107:81-83.
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"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene
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Zweier C, Albrecht B, Mitulla B, Behrens IK, Beese M, Gillessen-Kaesbach G, Rott HD, Rauch A. 2002. "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene. Am J Med Genet 108:177-181.
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Zweier, C.1
Albrecht, B.2
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Behrens, I.K.4
Beese, M.5
Gillessen-Kaesbach, G.6
Rott, H.D.7
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