Ding H - Search Results

1

Development of a community-based hearing loss prevention and control service model in Guangdong, China.

Liu C, Wang A, Huang Y, Zhang Y, Ding H, Wu J, Du L, Yang J, Mai F, Zeng Y, Liu L, Zhao X, Zhang C, Yin A. Liu C, et al. Among authors: ding h. BMC Public Health. 2019 Nov 29;19(1):1601. doi: 10.1186/s12889-019-7910-y. BMC Public Health. 2019. PMID: 31783833 Free PMC article.

2

The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing age.

Yin A, Liu C, Zhang Y, Wu J, Mai M, Ding H, Yang J, Zhang X. Yin A, et al. Among authors: ding h. BMC Med Genet. 2013 May 29;14:57. doi: 10.1186/1471-2350-14-57. BMC Med Genet. 2013. PMID: 23718755 Free PMC article.

3

Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families.

Yin A, Liu C, Zhang Y, Wu J, Mai M, Ding H, Yang J, Zhang X. Yin A, et al. Among authors: ding h. Int J Pediatr Otorhinolaryngol. 2014 Aug;78(8):1356-9. doi: 10.1016/j.ijporl.2014.05.030. Epub 2014 Jun 2. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24913939

4

[Gene diagnosis for a child with tuberous sclerosis].

Zhang Y, Ding H, Yin A, Zhang X. Zhang Y, et al. Among authors: ding h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):770-3. doi: 10.3760/cma.j.issn.1003-9406.2014.06.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449086 Chinese.

5

Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China.

Liu C, Zhang X, Wang J, Zhang Y, Wang A, Lu J, Huang Y, Liu S, Wu J, Du L, Yang J, Ding H, Liu L, Zhao X, Yin A. Liu C, et al. Among authors: ding h. Mol Cytogenet. 2019 Feb 18;12:7. doi: 10.1186/s13039-019-0420-x. eCollection 2019. Mol Cytogenet. 2019. PMID: 30820248 Free PMC article.

6

Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness - a case report for dual diagnosis.

Zhang Y, Zhang Y, Zhang VW, Zhang C, Ding H, Yin A. Zhang Y, et al. Among authors: ding h. BMC Pediatr. 2019 Oct 21;19(1):364. doi: 10.1186/s12887-019-1733-y. BMC Pediatr. 2019. PMID: 31638924 Free PMC article.

7

[Gene Diagnosis and Phenotypic Analysis of β-Thalassemia Caused from a Rare Synonymous Mutation CD29 (C>T)].

Qin DQ, DU L, Ding HK, Wang JC, Yuan TL, Yao CZ, Lan FF. Qin DQ, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Apr;28(2):577-582. doi: 10.19746/j.cnki.issn.1009-2137.2020.02.037. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020. PMID: 32319399 Chinese.

8

Variants c.677 C>T, c.1298 A>C in MTHFR, and c.66 A>G in MTRR Affect the Occurrence of Recurrent Pregnancy Loss in Chinese Women.

Zhang Y, Zhan W, Du Q, Wu L, Ding H, Liu F, Yin A. Zhang Y, et al. Among authors: ding h. Genet Test Mol Biomarkers. 2020 Nov;24(11):717-722. doi: 10.1089/gtmb.2020.0106. Epub 2020 Oct 29. Genet Test Mol Biomarkers. 2020. PMID: 33121283 Free PMC article.

9

[Analysis of clinical feature and genetic basis of a rare case with Olmsted syndrome].

Lu J, Hu R, Liu L, Ding H. Lu J, et al. Among authors: ding h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jul 10;38(7):674-677. doi: 10.3760/cma.j.cn511374-20200811-00597. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34247376 Chinese.

10

Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C).

Du L, Bao X, He W, Qin D, Wang J, Xiong Y, Shi X, Ding H, Yao C, Wu J. Du L, et al. Among authors: ding h. J Int Med Res. 2021 Jul;49(7):3000605211031429. doi: 10.1177/03000605211031429. J Int Med Res. 2021. PMID: 34334003 Free PMC article.

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