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Shprintzen-Goldberg syndrome associated with a novel missense mutation in TGFBR2

✍ Scribed by Maurice A.M. Van Steensel; Michel Van Geel; Lizelotte J.M.T. Parren; Constance T.R.M. Schrander-Stumpel; Dominique Marcus-Soekarman

No coin nor oath required. For personal study only.

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