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WNT5A mutations in patients with autosomal dominant Robinow syndrome., Person AD, Beiraghi S, Sieben CM, Hermanson S, Neumann AN, Robu ME, Schleiffarth JR, Billington CJ, van Bokhoven H, Hoogeboom JM, Mazzeu JF, Petryk A, Schimmenti LA, Brunner HG, Ekker SC, Lohr JL., Dev Dyn. January 1, 2010; 239 (1): 327-37.