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XB-ANAT-3329
Papers associated with pectoral appendage (and mecp2)
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Rare Diseases of Neurodevelopment: Maintain the Mystery or Use a Dazzling Tool for Investigation? The Case of Rett Syndrome., Ruffolo G., Neuroscience. July 15, 2020; 439 146-152. |
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Association of modified cytosines and the methylated DNA-binding protein MeCP2 with distinctive structural domains of lampbrush chromatin., Morgan GT., Chromosome Res. December 1, 2012; 20 (8): 925-42. |
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