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XB-ANAT-7
Papers associated with otic vesicle (and tgfbr2l)
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A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome., Rienhoff HY., Am J Med Genet A. August 1, 2013; 161A (8): 2040-6. |
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