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You searched for: Author/Creator Niu, Zhijie

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1. A de novo mutation of the SOX10 gene associated with inner ear malformation in a Guangxi family with Waardenburg syndrome type II. (June 2021)

4. Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I. Issue 9 (19th July 2022)

6. Apatinib for the treatment of metastatic or locoregionally recurrent nasopharyngeal carcinoma after failure of chemotherapy: A multicenter, single‐arm, prospective phase 2 study. Issue 17 (27th May 2021)

8. Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family. (September 2017)