WNT5A mutations in patients with autosomal dominant Robinow syndrome.
常染色体显性罗宾诺综合征患者的WNT5A基因突变
期刊:Developmental Dynamics
影响因子:1.5
doi:10.1002/dvdy.22156
Person Anthony D, Beiraghi Soraya, Sieben Christine M, Hermanson Spencer, Neumann Ann N, Robu Mara E, Schleiffarth J Robert, Billington Charles J Jr, van Bokhoven Hans, Hoogeboom Jeannette M, Mazzeu Juliana F, Petryk Anna, Schimmenti Lisa A, Brunner Han G, Ekker Stephen C, Lohr Jamie L
