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Did you mean guo ying chang (8 results)?
Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalities.
Li N, Xu Y, Chen H, Lin J, AlAbdi L, Bekheirnia MR, Li G, Gofin Y, Bekheirnia N, Faqeih E, Chen L, Chang G, Tang J, Yao R, Yu T, Wang X, Fu W, Fu Q, Shen Y, Alkuraya FS, Machol K, Wang J. Li N, et al. Among authors: chang g. EBioMedicine. 2024 Jan;99:104940. doi: 10.1016/j.ebiom.2023.104940. Epub 2023 Dec 27. EBioMedicine. 2024. PMID: 38154379 Free PMC article.
Molecular and Phenotypic Expansion of Alström Syndrome in Chinese Patients.
Zhang Q, Ding Y, Feng B, Tang Y, Chen Y, Wang Y, Chang G, Liu S, Wang J, Li Q, Fu L, Wang X. Zhang Q, et al. Among authors: chang g. Front Genet. 2022 Feb 8;13:808919. doi: 10.3389/fgene.2022.808919. eCollection 2022. Front Genet. 2022. PMID: 35211159 Free PMC article.
Clinical Profiles and Genetic Spectra of 814 Chinese Children With Short Stature.
Li X, Yao R, Chang G, Li Q, Song C, Li N, Ding Y, Li J, Chen Y, Wang Y, Huang X, Shen Y, Zhang H, Wang J, Wang X. Li X, et al. Among authors: chang g. J Clin Endocrinol Metab. 2022 Mar 24;107(4):972-985. doi: 10.1210/clinem/dgab863. J Clin Endocrinol Metab. 2022. PMID: 34850017 Free PMC article.
40 results