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XB--1000683
Papers associated with pfkm (and OMIM)
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Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects., Cowan JR, Tariq M, Shaw C, Rao M, Belmont JW, Lalani SR, Smolarek TA, Ware SM., Philos Trans R Soc Lond B Biol Sci. December 19, 2016; 371 (1710): |
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