Liu H - Search Results

1

[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. 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.

2

[Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene].

Li T, Hou Q, Wu D, Wang H, Liu H, Yang Y, Zhang C, Ding X, Liao S. Li T, et al. Among authors: liu h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):81-4. doi: 10.3760/cma.j.issn.1003-9406.2015.01.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636107 Chinese.

3

[Association of SPO11 and GST gene polymorphisms with idiopathic male infertility in ethnic Han Chinese].

Feng Z, Jing Z, Liu H, Liao S, Guo L, Mao C, Liu Y, Wu H, Gao J. Feng Z, et al. Among authors: liu y, liu h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):866-70. doi: 10.3760/cma.j.issn.1003-9406.2015.06.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663067 Chinese.

4

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: liu z, liu h. 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

5

[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: liu h, liu s. 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.

6

[Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene].

Liu H, Huang J, Jiang Y, Guo L, Xiao H, Wang H. Liu H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jan 10;37(1):17-20. doi: 10.3760/cma.j.issn.1003-9406.2020.01.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 31922588 Chinese.

7

[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: liu 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.

8

[Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate].

Zhang M, Huang J, Shi F, He J, Xiao H, Wu D, Wang H, Liu H. Zhang M, et al. Among authors: liu h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jan 10;38(1):52-55. doi: 10.3760/cma.j.cn511374-20200308-00144. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33423258 Chinese.

9

[Efficiency of multiplex ligation-dependent probe amplification combined with short tandem repeat linkage analysis for the prenatal diagnosis for Duchenne muscular dystrophy].

Li T, Wu D, Hou QF, Wang L, Guo QN, Kang B, Liu HY, Yang K, Ding XB, Liao SX. Li T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):40-4. doi: 10.3760/cma.j.issn.1003-9406.2013.01.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450477 Chinese.

10

Collagen Type I Alpha 1 Mutation Causes Osteogenesis Imperfecta from Mild to Perinatal Death in a Chinese Family.

Liu HY, Huang J, Wu D, Li T, Guo LJ, Guo QN, Wang HD, Wang RL, Wang Y. Liu HY, et al. Chin Med J (Engl). 2016 Jan 5;129(1):88-91. doi: 10.4103/0366-6999.172600. Chin Med J (Engl). 2016. PMID: 26712438 Free PMC article. No abstract available.

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