Huo X - Search Results

1

Novel autosomal recessive SINO syndrome-associated KIDINS220 variants provide insight into the genotype-phenotype correlation.

Yang W, Wang S, Huo X, Yang K, Guo Z, Li Y, Ji X, Hao B, Liao S. Yang W, et al. Among authors: huo x. Heliyon. 2024 Sep 2;10(17):e37355. doi: 10.1016/j.heliyon.2024.e37355. eCollection 2024 Sep 15. Heliyon. 2024. PMID: 39296002 Free PMC article.

2

A Novel Variant of the KIF11 Gene, c.2922G>T, Is Associated with Microcephaly by Affecting RNA Splicing.

Guo Z, Huo X, Wu D, Hao B, Liao S. Guo Z, et al. Among authors: huo x. Dev Neurosci. 2022;44(2):113-120. doi: 10.1159/000518923. Epub 2021 Aug 31. Dev Neurosci. 2022. PMID: 34965526

3

[Analysis of CNTNAP1 gene variants in a Chinese pedigree affected with lethal congenital contracture syndrome type 7].

Zhang Y, Yang S, Huo X, Liao S, Hou Q. Zhang Y, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Feb 10;39(2):194-197. doi: 10.3760/cma.j.cn511374-20201021-00739. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35076918 Chinese.

4

Deep phenotyping and whole-exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders.

Wang Q, Tang X, Yang K, Huo X, Zhang H, Ding K, Liao S. Wang Q, et al. Among authors: huo x. Mol Genet Genomic Med. 2022 May;10(5):e1918. doi: 10.1002/mgg3.1918. Epub 2022 Mar 10. Mol Genet Genomic Med. 2022. PMID: 35266334 Free PMC article.

5

[Clinical features and genetic analysis of two Chinese pedigrees affected with Joubert syndrome].

Zhao D, Chu Y, Yang K, Huo X, Lei X, Yang Y, Zhang C, Xiao H, Liao S. Zhao D, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Jan 10;40(1):21-25. doi: 10.3760/cma.j.cn511374-20220122-00055. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36584995 Chinese.

6

[Genetic diagnosis of a child with Smith-Magenis syndrome].

Gao Y, Wu D, Huo X, Zhang M, Hou Q, Wang H, Liao S. Gao Y, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):724-726. doi: 10.3760/cma.j.issn.1003-9406.2019.07.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302921 Chinese.

7

[Genetic analysis of a pedigree affected with Bartter's syndrome].

Yang K, Huo X, Zhang Y, Zhang M, Gao Y, Wu D, Lou G, Qi N, Zhang B, Wang D. Yang K, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):701-703. doi: 10.3760/cma.j.issn.1003-9406.2019.07.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302915 Chinese.

8

[Genetic analysis of a child with atypical Williams-Beuren syndrome presenting as supravalvular aortic stenosis].

Wu D, Zhang M, Gao Y, Huo X, Xiao H, Zhang Q, Kang B, Wang X, Liao S. Wu D, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):475-478. doi: 10.3760/cma.j.issn.1003-9406.2020.04.028. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219841 Chinese.

9

[Phenotypic and genetic analysis of a child carrying a 17q11.2 microdeletion].

Wang H, Feng Z, Yang K, Gao Y, Huo X, Qin L, Lou G. Wang H, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):695-698. doi: 10.3760/cma.j.issn.1003-9406.2017.05.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981936 Chinese.

10

[Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan].

Wang H, Kang B, Gao Y, Huo X, Li T, Guo Q, Zhu B, Liao S. Wang H, et al. Among authors: huo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):266-269. doi: 10.3760/cma.j.issn.1003-9406.2017.02.026. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397234 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,027 results

Search Page

Filters