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 Jr, van Bokhoven H, Hoogeboom JM, Mazzeu JF, Petryk A, Schimmenti LA, Brunner HG, Ekker SC, Lohr JL.
Person AD, et al.
Dev Dyn. 2010 Jan;239(1):327-37. doi: 10.1002/dvdy.22156.
Dev Dyn. 2010.
PMID: 19918918
Free PMC article.