Papers associated with fam3b
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Identification of rare loss-of-function variants in FAM3B associated with non-syndromic orofacial clefts., Zhao H, He Q, Wu X, Liang X, Jiao Y, Zhang Y, Bao S, Xu L, Hou Y, Zhu X, Ding Y., Genomics. May 1, 2023; 115 (3): 110630.