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10.13201/j.issn.2096-7993.2021.04.020

[Obstructive sleep apnea in microtia children with maxillofacial dysostosis].



Nager syndrome in patient lacking acrofacial dysostosis: Expanding the phenotypic spectrum of SF3B4‐related disease


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10.1016/j.ydbio.2021.04.002

Molecular mechanisms of hearing loss in Nager syndrome.


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10.26574/maedica.2020.16.1.140

Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome.


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10.1016/j.amsu.2021.102896

Possible autosomal recessive inheritance in a neonate with Nager syndrome: Case report


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10.1097/SCS.0000000000007533

Alloplastic Temporomandibular Joint Reconstruction in Congenital Craniofacial Deformities



The role of double-step advancement genioplasty and bilateral coronoidectomy in Nager Syndrome: A case report.



A Case of Nager Syndrome Diagnosed Before Birth.



The final demise of Rodriguez lethal acrofacial dysostosis: A case report and review of the literature


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10.1016/j.ijporl.2019.109842

Associated syndromes in patients with Pierre Robin Sequence.


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10.1073/pnas.1901742116

Component of splicing factor SF3b plays a key role in translational control of polyribosomes on the endoplasmic reticulum


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