Hou Q - Search Results

1

Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome.

Zhang Q, Yang S, Chen X, Wang H, Li K, Zhang C, Liao S, Qin L, Hou Q. Zhang Q, et al. Among authors: hou q. Front Genet. 2023 Sep 6;14:1252873. doi: 10.3389/fgene.2023.1252873. eCollection 2023. Front Genet. 2023. PMID: 37736303 Free PMC article.

2

[Mutation analysis and prenatal diagnosis of COL1A1 gene in a Chinese family with type I osteogenesis imperfecta].

Zhang H, Wu D, Hou Q, Liu Z, Qin L, Liao S. Zhang H, et al. Among authors: hou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):730-2. doi: 10.3760/cma.j.issn.1003-9406.2014.06.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449076 Chinese.

3

A novel MIP mutation in familial congenital nuclear cataracts.

Qin L, Guo L, Wang H, Li T, Lou G, Guo Q, Hou Q, Liu H, Liao S, Liu Z. Qin L, et al. Among authors: hou q. Eur J Med Genet. 2016 Sep;59(9):488-91. doi: 10.1016/j.ejmg.2016.07.002. Epub 2016 Jul 22. Eur J Med Genet. 2016. PMID: 27456987

4

Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome.

Qin L, Li X, Hou Q, Wang H, Lou G, Li T, Wang L, Liu H, Li X, Liao S. Qin L, et al. Among authors: hou q. Clin Chim Acta. 2017 Oct;473:26-31. doi: 10.1016/j.cca.2017.08.007. Epub 2017 Aug 10. Clin Chim Acta. 2017. PMID: 28803747

5

[Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis].

Lou G, Yang K, Qin L, Zhang Y, Wang H, Hou Q, He M, Liao S. Lou G, et al. Among authors: hou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):91-95. doi: 10.3760/cma.j.issn.1003-9406.2018.01.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419870 Chinese.

6

[Analysis of WAS gene mutation in a Chinese family affected with Wiskott-Aldrich syndrome].

Shi W, Hou Q, Zhang H, Lou G, Zhang Y, Liao S. Shi W, et al. Among authors: hou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):207-209. doi: 10.3760/cma.j.issn.1003-9406.2018.02.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652993 Chinese.

7

[Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome].

Chu Y, Hou Q, Wu D, Lou G, Yang K, Guo L, Qi N, Duan X, Wang W, Qin L, Liao S. Chu Y, et al. Among authors: hou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Oct 10;36(10):1022-1024. doi: 10.3760/cma.j.issn.1003-9406.2019.10.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31598951 Chinese.

8

[Identification of SPAST gene variant in a pedigree affected with hereditary spastic paraplegia type 4].

Qi N, Ma M, Yang K, Lou G, Qin L, Hou Q, Zhang Y, Liao S. Qi N, et al. Among authors: hou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Nov 10;37(11):1261-1264. doi: 10.3760/cma.j.cn511374-20191120-00592. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33179235 Chinese.

9

[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: hou q. 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.

10

[Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion].

Wu D, Shi W, Wang H, Hou Q, Zhang H, Li T, Zhang C, Yang Y, Liao S. Wu D, et al. Among authors: hou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):718-721. doi: 10.3760/cma.j.issn.1003-9406.2017.05.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981941 Chinese.

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