Lv7
5000 积分 2021-10-23 加入
Craniofacial and intraoral phenotype of Robinow syndrome forms
2小时前
待确认
[Wnt Signaling and Skeletal Dysplasias.]
8天前
已关闭
Autosomal Dominant Robinow Syndrome
8天前
已关闭
Prevalence and clinical features of Costello syndrome and cardio‐facio‐cutaneous syndrome in Japan: Findings from a nationwide epidemiological survey
1个月前
已完结
Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation
1个月前
已完结
DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathway
1个月前
已完结
DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathway
1个月前
已完结
Abnormal WNT5A Signaling Causes Mandibular Hypoplasia in Robinow Syndrome
1个月前
已完结
Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation
1个月前
已完结
Robinow syndrome, Cockayne syndrome, and Pfeiffer syndrome: an overview of physical, neurological, and oral characteristics
2个月前
已关闭
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