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Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.
Sci Adv. 2023 Apr 28;9(17):eade0631. doi: 10.1126/sciadv.ade0631. Epub 2023 Apr 26.
Sci Adv. 2023.
PMID: 37126546
Free PMC article.
Preterm Birth and Birth Weight and the Risk of Type 1 Diabetes in Chinese Children.
Huang K, Si S, Chen R, Wang C, Chen S, Liang Y, Yao H, Zheng R, Liu F, Cao B, Su Z, Mireguli M, Luo F, Li P, Du H, Zhu M, Yang Y, Cui L, Yu Y, Fu J.
Huang K, et al. Among authors: mireguli m.
Front Endocrinol (Lausanne). 2021 Apr 14;12:603277. doi: 10.3389/fendo.2021.603277. eCollection 2021.
Front Endocrinol (Lausanne). 2021.
PMID: 33935963
Free PMC article.
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A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children.
Lin L, Li M, Luo J, Li P, Zhou S, Yang Y, Chen K, Weng Y, Ge X, Mireguli M, Wei H, Yang H, Li G, Sun Y, Cui L, Zhang S, Chen J, Zeng G, Xu L, Luo X, Shen Y.
Lin L, et al. Among authors: mireguli m.
J Clin Endocrinol Metab. 2021 Jun 16;106(7):e2711-e2719. doi: 10.1210/clinem/dgab088.
J Clin Endocrinol Metab. 2021.
PMID: 33606014
Free PMC article.
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CNV profiles of Chinese pediatric patients with developmental disorders.
Yuan H, Shangguan S, Li Z, Luo J, Su J, Yao R, Zhang S, Liang C, Chen Q, Gao Z, Zhu Y, Zhang S, Li W, Lu W, Zhang Y, Xie H, Liu F, Wang Q, Lin Y, Liu L, Wang X, Liang L, Zhong J, Li H, Qiu H, Zhang H, Yan M, Mireguli M, Liu Y, Zhang D, Wang H, Lv H, Xie B, Gui C, Cui X, Zou L, Wang J, Gusella JF, Shen Y, Chen X.
Yuan H, et al. Among authors: mireguli m.
Genet Med. 2021 Apr;23(4):669-678. doi: 10.1038/s41436-020-01048-y. Epub 2021 Jan 5.
Genet Med. 2021.
PMID: 33402738
Free article.
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[Genotypes and phenotypes of nine Uygur children with osteogenesis imperfecta in Xinjiang].
Luo YF, Dilihuma J, Sun GH, Reyilanmu B, Liang L, Du XY, Mireguli M.
Luo YF, et al. Among authors: mireguli m.
Zhonghua Er Ke Za Zhi. 2020 Feb 2;58(2):135-139. doi: 10.3760/cma.j.issn.0578-1310.2020.02.013.
Zhonghua Er Ke Za Zhi. 2020.
PMID: 32102151
Chinese.
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[Clinical features and INS mutations of an infant with neonatal diabetes mellitus].
Luo YF, Liang L, Sun GH, Reyilanmu B, DU XY, Cao C, Zhao ZZ, Dilihuma J, Tang XD, Mireguli M.
Luo YF, et al. Among authors: mireguli m.
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Nov;20(11):955-957. doi: 10.7499/j.issn.1008-8830.2018.11.015.
Zhongguo Dang Dai Er Ke Za Zhi. 2018.
PMID: 30477630
Free PMC article.
Chinese.
No abstract available.
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Novel Compound Heterozygous Variants in the LHCGR Gene in a Genetically Male Patient with Female External Genitalia.
Yan M, Dilihuma J, Luo Y, Reyilanmu B, Shen Y, Mireguli M.
Yan M, et al. Among authors: mireguli m.
J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):211-217. doi: 10.4274/jcrpe.galenos.2018.2018.0197. Epub 2018 Nov 16.
J Clin Res Pediatr Endocrinol. 2019.
PMID: 30444213
Free PMC article.
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