Wu DW - Search Results

1

[Polymicrogyria associated with ADGRG1 gene variations in a child].

Liu XR, Jiang TJ, Yang XH, Wu DW, Tong F, Gao F. Liu XR, et al. Among authors: wu dw. Zhonghua Er Ke Za Zhi. 2024 Nov 2;62(11):1110-1112. doi: 10.3760/cma.j.cn112140-20240621-00420. Zhonghua Er Ke Za Zhi. 2024. PMID: 39429086 Chinese.

2

[Analysis of newborn screening for galactosemia and genotype-phenotype of confirmed galatosemia cases].

Yang RL, Tong F, Hong F, Qian GL, Wu DW, Zhao ZY. Yang RL, et al. Among authors: wu dw. Zhonghua Er Ke Za Zhi. 2017 Feb 2;55(2):104-109. doi: 10.3760/cma.j.issn.0578-1310.2017.02.010. Zhonghua Er Ke Za Zhi. 2017. PMID: 28173647 Chinese.

3

[A case of Wiedemann-Steiner syndrome caused by a novel variation of the KMT2A gene].

Wang JL, Huang K, Wu W, Zhu MQ, Lin H, Wu DW, Dong GP, Fu JF. Wang JL, et al. Among authors: wu w, wu dw. Zhonghua Er Ke Za Zhi. 2021 Jun 2;59(6):516-518. doi: 10.3760/cma.j.cn112140-20201231-01145. Zhonghua Er Ke Za Zhi. 2021. PMID: 34102828 Chinese.

4

FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.

Zhang JY, Wu DW, Yang RL, Zhu L, Jiang MY, Wang WJ, Li XK, Jiang XL, Tong F, Shu Q. Zhang JY, et al. Among authors: wu dw. World J Pediatr. 2021 Dec;17(6):653-658. doi: 10.1007/s12519-021-00473-6. Epub 2021 Nov 5. World J Pediatr. 2021. PMID: 34738199

5

Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.

Tong F, Wang J, Xiao R, Wu BB, Zou CC, Wu DW, Wang H, Zou H, Han LS, Yang L, Zou L, Hei MY, Yang RL, Yuan TM, Wen W, Huang XW, Gu XF, Yang YL, Huang YL, Zhang YJ, Yu YG, Xu ZF, Zhou WH, Zhao ZY. Tong F, et al. Among authors: wu bb, wu dw. World J Pediatr. 2022 Apr;18(4):235-242. doi: 10.1007/s12519-022-00522-8. Epub 2022 Mar 15. World J Pediatr. 2022. PMID: 35292922 No abstract available.

6

A multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in China.

Yang RL, Qian GL, Wu DW, Miao JK, Yang X, Wu BQ, Yan YQ, Li HB, Mao XM, He J, Shen H, Zou H, Xue SY, Li XZ, Niu TT, Xiao R, Zhao ZY. Yang RL, et al. Among authors: wu bq, wu dw. World J Pediatr. 2023 Jul;19(7):663-673. doi: 10.1007/s12519-022-00670-x. Epub 2023 Feb 27. World J Pediatr. 2023. PMID: 36847978 Free PMC article.

7

Genotypic and phenotypic spectrum of maple syrup urine disease in Zhejiang of China.

Yang X, Yang R, Zhang T, Tan DJ, Pan R, Chen Z, Wu D, Chen C, Xu Y, Zhang L, Li X, Shu Q, Hu L. Yang X, et al. QJM. 2024 Oct 1;117(10):717-727. doi: 10.1093/qjmed/hcae104. QJM. 2024. PMID: 38837343 Free PMC article.

8

Comprehensive newborn screening for severe combined immunodeficiency, X-linked agammaglobulinemia, and spinal muscular atrophy: the Chinese experience.

Chen C, Zhang C, Wu DW, Wang BY, Xiao R, Huang XL, Yang X, Gao ZG, Yang RL. Chen C, et al. Among authors: wu dw. World J Pediatr. 2024 Dec;20(12):1270-1282. doi: 10.1007/s12519-024-00846-7. Epub 2024 Nov 5. World J Pediatr. 2024. PMID: 39500858 Free PMC article.

9

[Preliminary investigation of gender assignment in 46,XY disorders of sex development with severe male undermasculinisation].

Wu DH, Tian HJ, Yuan JN, Dong GP, Wu DW, Yang RW, Sun LY, Tang DX, Fu JF. Wu DH, et al. Among authors: wu dw. Zhonghua Er Ke Za Zhi. 2019 Oct 2;57(10):786-791. doi: 10.3760/cma.j.issn.0578-1310.2019.10.011. Zhonghua Er Ke Za Zhi. 2019. PMID: 31594066 Chinese.

10

[Relationship between 22q11 microdeletion syndrome and congenital heart disease].

Qin YF, Xie CH, Yang JB, Wu DW, Shao J, Zhao ZY. Qin YF, et al. Among authors: wu dw. Zhonghua Xin Xue Guan Bing Za Zhi. 2011 Jul;39(7):631-5. Zhonghua Xin Xue Guan Bing Za Zhi. 2011. PMID: 22088244 Chinese.

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