Xiao H - Search Results

1

[Genetic analysis of 90 families affected with spinal muscular atrophy].

Li T, Lyu X, Xu P, Zou J, Xiao H, Guo Q, Wang H, Liu H. Li T, et al. Among authors: xiao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Feb 10;37(2):116-122. doi: 10.3760/cma.j.issn.1003-9406.2020.02.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32034734 Chinese.

2

DNA methylation study of fetus genome through a genome-wide analysis.

Wang HD, Hou QF, Guo QN, Li T, Wu D, Zhang XP, Chu Y, He M, Xiao H, Guo LJ, Yang K, Liao SX, Zhu BF. Wang HD, et al. Among authors: xiao h. BMC Med Genomics. 2014 Apr 15;7:18. doi: 10.1186/1755-8794-7-18. BMC Med Genomics. 2014. PMID: 24731722 Free PMC article.

3

[Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].

Wu D, Wang H, Zhang H, Hou Q, Qin L, Wang T, Xiao H, Liao S, Wang Y. Wu D, et al. Among authors: xiao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):823-6. doi: 10.3760/cma.j.issn.1003-9406.2015.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663057 Chinese.

4

[Analysis of PRRT2 gene mutations in a Chinese family affected with paroxysmal kinesigenic dyskinesia].

Zhang H, Shi W, Xiao H, Wu D, Qin L, Liao S. Zhang H, et al. Among authors: xiao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Feb;33(1):61-3. doi: 10.3760/cma.j.issn.1003-9406.2016.01.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 26829736 Chinese.

5

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome.

Shi WL, Liu ZZ, Wang HD, Wu D, Zhang H, Xiao H, Chu Y, Hou QF, Liao SX. Shi WL, et al. Among authors: xiao h. J Biomed Sci. 2016 Jun 7;23(1):48. doi: 10.1186/s12929-016-0265-0. J Biomed Sci. 2016. PMID: 27266699 Free PMC article.

6

[Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia].

Liu H, Li T, Wang H, Guo L, Wu D, Xiao H, Guo Q, Wang T. Liu H, et al. Among authors: xiao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):629-32. doi: 10.3760/cma.j.issn.1003-9406.2016.05.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577209 Chinese.

7

Diagnosis with Multiple Epiphyseal Dysplasia Using Whole-exome Sequencing in a Chinese Family.

Liu HY, Xiao JF, Huang J, Wang Y, Wu D, Li T, Wang HD, Guo LJ, Guo QN, Xiao H, Lyu X, Yu ZH. Liu HY, et al. Among authors: xiao h, xiao jf. Chin Med J (Engl). 2017 Jan 5;130(1):104-107. doi: 10.4103/0366-6999.196568. Chin Med J (Engl). 2017. PMID: 28051032 Free PMC article. No abstract available.

8

Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect.

Guo QN, Wang HD, Tie LZ, Li T, Xiao H, Long JG, Liao SX. Guo QN, et al. Among authors: xiao h. Biomed Res Int. 2017;2017:3043476. doi: 10.1155/2017/3043476. Epub 2017 Jul 3. Biomed Res Int. 2017. PMID: 28758112 Free PMC article. Clinical Trial.

9

[Genetic and prenatal diagnosis for a haemophilia A family with two novel mutations of F8 gene].

Li T, Hou Q, Liu H, Xiao H, Zhang B, Liu S, Yang Y, Zhang C, Ding X, Liao S. Li T, et al. Among authors: xiao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):486-489. doi: 10.3760/cma.j.issn.1003-9406.2017.04.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777843 Chinese.

10

Maternal natural killer cell immunoglobulin receptor genes and human leukocyte antigen-C ligands influence recurrent spontaneous abortion in the Han Chinese population.

Su N, Wang H, Zhang B, Kang Y, Guo Q, Xiao H, Yang H, Liao S. Su N, et al. Among authors: xiao h. Exp Ther Med. 2018 Jan;15(1):327-337. doi: 10.3892/etm.2017.5406. Epub 2017 Oct 31. Exp Ther Med. 2018. PMID: 29387191 Free PMC article.

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