Shi HR - Search Results

1

[Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families].

Wu Q, Shi HR, Liu N, Lu N, Jiang M, Zhao ZH, Kong XD. Wu Q, et al. Among authors: shi hr. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):377-81. doi: 10.3760/cma.j.issn.1003-9406.2012.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875490 Chinese.

2

Tyrosinase gene mutations in the Chinese Han population with OCA1.

Liu N, Kong XD, Shi HR, Wu QH, Jiang M. Liu N, et al. Among authors: shi hr. Genet Res (Camb). 2014 Nov 12;96:e14. doi: 10.1017/S0016672314000160. Genet Res (Camb). 2014. PMID: 25577957 Free PMC article.

3

[Detection of ED1 gene mutations in six pedigrees with hypohidrotic ectodermal dysplasia].

Wu QH, Shi HR, Liu BC, Zhao ZH, Jiang M, Lu N, Kong XD. Wu QH, et al. Among authors: shi hr. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):447-51. doi: 10.3760/cma.j.issn.1003-9406.2012.04.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875504 Chinese.

4

[Mutation analysis and prenatal diagnosis of a Chinese family with X-linked severe combined immunodeficiency].

Wu QH, Shi HR, Liu N, Jiang M, Lu N, Zhao ZH, Kong XD. Wu QH, et al. Among authors: shi hr. Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):851-4. Zhonghua Er Ke Za Zhi. 2012. PMID: 23302618 Chinese.

5

[Mutation analysis and first-trimester prenatal diagnosis for a Chinese family with hidrotic ectodermal dysplasia].

Liu N, Shi HR, Wu QH, Jiang M, Kong XD. Liu N, et al. Among authors: shi hr. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):407-9. doi: 10.3760/cma.j.issn.1003-9406.2013.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926005 Chinese.

6

[Mutation analysis of phenylalanine hydroxylase gene in patients w ith phenylketonuria in Henan province].

GUO HJ, ZHAO ZH, JIANG M, SHI HR, KONG XD. GUO HJ, et al. Among authors: shi hr. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):142-6. doi: 10.3760/cma.j.issn.1003-9406.2011.02.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21462123 Chinese.

7

A novel 1-bp deletion mutation of the EDA gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia.

Kong XD, Liu N, Shi HR, Yang YX. Kong XD, et al. Among authors: shi hr. J Dermatol. 2014 Jul;41(7):659-61. doi: 10.1111/1346-8138.12431. J Dermatol. 2014. PMID: 24985548 No abstract available.

8

Value of frozen section examination in diagnosis and treatment of high-grade cervical intraepithelial neoplasia.

Ren F, Feng W, Shi HR, Wu QH, Chen ZM. Ren F, et al. Among authors: shi hr. Chin Med J (Engl). 2012 Jul;125(14):2462-5. Chin Med J (Engl). 2012. PMID: 22882922

9

Mutation analysis and prenatal diagnosis in a Chinese family with succinic semialdehyde dehydrogenase and a systematic review of the literature of reported ALDH5A1 mutations.

Liu N, Kong XD, Kan QC, Shi HR, Wu QH, Zhuo ZH, Bai QL, Jiang M. Liu N, et al. Among authors: shi hr. J Perinat Med. 2016 May 1;44(4):441-51. doi: 10.1515/jpm-2014-0164. J Perinat Med. 2016. PMID: 25431891 Review.

10

[Expression and clinical significance of endostatin and vascular endothelial growth factor in ovarian carcinoma].

Shi HR, Song WJ, Chen ZM, Wu QH. Shi HR, et al. Ai Zheng. 2005 Sep;24(9):1127-31. Ai Zheng. 2005. PMID: 16159439 Chinese.

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