Hu H - Search Results

1

Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.

Hu H, Wu L, Feng Y, Pan Q, Long Z, Li J, Dai H, Xia K, Liang D, Niikawa N, Xia J. Hu H, et al. J Hum Genet. 2007;52(6):492-497. doi: 10.1007/s10038-007-0139-0. Epub 2007 Apr 19. J Hum Genet. 2007. PMID: 17443271

2

Molecular analysis of SLC26A4 gene in a Chinese deafness family.

Hu H, Liang DS, Wu LQ, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):376-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086271

3

[Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation].

Hu H, Wu LQ, Liang DS, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Zhonghua Fu Chan Ke Za Zhi. 2005 Sep;40(9):591-4. Zhonghua Fu Chan Ke Za Zhi. 2005. PMID: 16202311 Chinese.

4

[Rapid detection of the hot spot gene mutations in Chinese patients with nonsyndromic hearing loss by polymerase chain reaction-restrictive fragment length polymorphism].

Zhao J, Wu LQ, Feng Y, Hu H, Pan Q, Xiong LQ, Liang DS. Zhao J, et al. Among authors: hu h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):518-20. doi: 10.3760/cma.j.issn.1003-9406.2009.05.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806571 Chinese.

5

[Research progress in nonsyndromic sensorineural hearing loss associated genes].

Hu H, Wu LQ, Liang DS, Xia JH. Hu H, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Aug;40(8):633-7. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005. PMID: 16270893 Review. Chinese. No abstract available.

6

[Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR].

Wu YL, Wu LQ, Li YP, Liu DE, Zeng Q, Zhu HY, Pan Q, Liang DS, Hu H, Long ZG, Li J, Dai HP, Xia K, Xia JH. Wu YL, et al. Among authors: hu h. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Apr;32(2):246-51. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007. PMID: 17478931 Chinese.

7

[Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia].

Hu LP, Liu NH, Pan Q, Liang DS, Long ZG, Hu H, Zhu HY, Dai HP, Cai F, Wu LQ, Xia K, Xia JH. Hu LP, et al. Among authors: hu h. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Apr;32(2):241-5. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007. PMID: 17478930 Chinese.

8

XRCC2 mutation causes meiotic arrest, azoospermia and infertility.

Yang Y, Guo J, Dai L, Zhu Y, Hu H, Tan L, Chen W, Liang D, He J, Tu M, Wang K, Wu L. Yang Y, et al. Among authors: hu h. J Med Genet. 2018 Sep;55(9):628-636. doi: 10.1136/jmedgenet-2017-105145. Epub 2018 Jul 24. J Med Genet. 2018. PMID: 30042186 Free PMC article.

9

Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening.

Li CX, Pan Q, Guo YG, Li Y, Gao HF, Zhang D, Hu H, Xing WL, Mitchelson K, Xia K, Dai P, Cheng J. Li CX, et al. Among authors: hu h. Hum Mutat. 2008 Feb;29(2):306-14. doi: 10.1002/humu.20622. Hum Mutat. 2008. PMID: 18161878 Free PMC article.

10

[A novel mutation in Mitf gene leads to a patient with Waardenburg syndrome type II].

Feng Y, Liu ZZ, Hu H. Feng Y, et al. Among authors: hu h. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Oct;42(10):787-8. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18229597 Chinese. No abstract available.

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