Wang D - Search Results

1

Genotypic and phenotypic characteristics of 12 chinese children with glycogen storage diseases.

Dong R, Wei X, Zhang K, Song F, Lv Y, Gao M, Wang D, Ma J, Gai Z, Liu Y. Dong R, et al. Among authors: wang d. Front Genet. 2022 Aug 29;13:932760. doi: 10.3389/fgene.2022.932760. eCollection 2022. Front Genet. 2022. PMID: 36105079 Free PMC article.

2

Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.

Wang D, Song L, Shen L, Zhang K, Lv Y, Gao M, Ma J, Wan Y, Gai Z, Liu Y. Wang D, et al. Front Pharmacol. 2021 Jul 16;12:644352. doi: 10.3389/fphar.2021.644352. eCollection 2021. Front Pharmacol. 2021. PMID: 34335240 Free PMC article.

3

Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.

Zhang K, Liu S, Gu W, Lv Y, Yu H, Gao M, Wang D, Zhao J, Li X, Gai Z, Zhao S, Liu Y, Yuan Y. Zhang K, et al. Among authors: wang d. Front Genet. 2021 Aug 24;12:630650. doi: 10.3389/fgene.2021.630650. eCollection 2021. Front Genet. 2021. PMID: 34504512 Free PMC article.

4

Analysis of clinical and genetic characteristics in 10 Chinese individuals with Cornelia de Lange syndrome and literature review.

Liu C, Li X, Cui J, Dong R, Lv Y, Wang D, Zhang H, Li X, Li Z, Ma J, Liu Y, Gai Z. Liu C, et al. Among authors: wang d. Mol Genet Genomic Med. 2020 Oct;8(10):e1471. doi: 10.1002/mgg3.1471. Epub 2020 Aug 27. Mol Genet Genomic Med. 2020. PMID: 32856424 Free PMC article. Review.

5

[Clinical and genetic analysis of a patient with Angelman syndrome due to a frameshift variant of UBE3A gene].

Gao Z, Lyu Y, Zhang K, Gao M, Ma J, Wang D, Gai Z, Liu Y. Gao Z, et al. Among authors: wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Oct 10;37(10):1120-1123. doi: 10.3760/cma.j.cn511374-20190912-00469. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32924115 Chinese.

6

[Genetic analysis of a case with Pitt-Hopkins syndrome due to variant of TCF4 gene].

Ma J, Zhang H, Zhang K, Lyu Y, Gao M, Wang D, Gai Z, Liu Y. Ma J, et al. Among authors: wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Nov 10;37(11):1253-1256. doi: 10.3760/cma.j.cn511374-20190725-00372. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33179233 Chinese.

7

[Identification of a GNB1 gene variant in a child with autosomal dominant mental retardation 42].

Ren Y, Lyu Y, Ma J, Wang D, Zhang G, Liu Y, Gai Z. Ren Y, et al. Among authors: wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jun 10;38(6):565-568. doi: 10.3760/cma.j.cn511374-20200121-00044. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34096027 Chinese.

8

[Analysis of ADNP gene variant in a child with Helsmoortel-van der Aa syndrome].

Ma J, Ma H, Zhang K, Lyu Y, Gao M, Wang D, Gai Z, Liu Y. Ma J, et al. Among authors: wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):428-432. doi: 10.3760/cma.j.cn511374-20201113-00797. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446982 Chinese.

9

[Analysis of PRX gene variants in a child with Charcot-Marie-Tooth disease type 4F].

Yang Y, Ye S, Lyu Y, Xin H, Gao M, Ma J, Wang D, Gai Z, Liu Y. Yang Y, et al. Among authors: wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jul 10;39(7):749-753. doi: 10.3760/cma.j.cn511374-20210311-00221. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35810435 Chinese.

10

[Analysis of TNPO3 gene variant and clinical phenotype in a neonate with limb-girdle muscular dystrophies form 1F].

Gao M, Hou L, Zhang K, Lyu Y, Ma J, Wang D, Gai Z, Liu Y. Gao M, et al. Among authors: wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Sep 10;39(9):979-982. doi: 10.3760/cma.j.cn511374-20210804-00649. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36082569 Chinese.

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