Yu D - Search Results

1

Genetic analysis and prenatal diagnosis of short-rib thoracic dysplasia 3 with or without polydactyly caused by compound heterozygous variants of DYNC2H1 gene in four Chinese families.

Fang Y, Li S, Yu D. Fang Y, et al. Among authors: yu d. Front Genet. 2023 Mar 17;14:1075187. doi: 10.3389/fgene.2023.1075187. eCollection 2023. Front Genet. 2023. PMID: 37007936 Free PMC article.

2

[Evaluation of Down's syndrome screening methods using maternal serum biochemistry in the second trimester pregnancy].

Yu DY, Fu P, Zhang ZH, Wang F, Han MY, Ren HY, Zhao W, Zhang K, Li S, Jiang N. Yu DY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Jun;28(3):332-5. doi: 10.3760/cma.j.issn.1003-9406.2011.03.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21644235 Chinese.

3

[Establishment and application of median serum markers for second trimester screening in Qingdao region].

Yu DY, Wang F, Liu Q, Jiang N, Zhao W, Ren HY, Han MY, Zhang K, Li S, Ouyang QQ, Nie Q. Yu DY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):587-91. doi: 10.3760/cma.j.issn.1003-9406.2012.05.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042400 Chinese.

4

[Infantile spasm associated with 5q14.3 microdeletion syndrome: clinical and genetic characterization of a core family].

Yu D, Li S, Jiang N. Yu D, et al. Zhonghua Er Ke Za Zhi. 2015 Feb;53(2):140-2. Zhonghua Er Ke Za Zhi. 2015. PMID: 25876691 Chinese.

5

A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient.

Liang S, Jiang N, Li S, Jiang X, Yu D. Liang S, et al. Among authors: yu d. Mol Cytogenet. 2017 Jun 14;10:23. doi: 10.1186/s13039-017-0324-6. eCollection 2017. Mol Cytogenet. 2017. PMID: 28630650 Free PMC article.

6

Novel chromosomal microduplications associated with dolichocephaly craniosynostosis: A case report.

Yu D, Li S, Liu Q, Zhang K. Yu D, et al. Medicine (Baltimore). 2017 Dec;96(49):e8729. doi: 10.1097/MD.0000000000008729. Medicine (Baltimore). 2017. PMID: 29245229 Free PMC article.

7

[False positive non-invasive prenatal testing results due to vanishing twins].

Yu T, Li S, Zhao W, Yu D. Yu T, et al. Among authors: yu d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Apr 10;36(4):327-330. doi: 10.3760/cma.j.issn.1003-9406.2019.04.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30950018 Chinese.

8

[Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].

Zhao W, Jiang N, Li S, Li JS, Miao Y, Liang SY, Yu DY. Zhao W, et al. Among authors: yu dy. Zhonghua Fu Chan Ke Za Zhi. 2019 Apr 25;54(4):226-231. doi: 10.3760/cma.j.issn.0529-567x.2019.04.003. Zhonghua Fu Chan Ke Za Zhi. 2019. PMID: 31006187 Chinese.

9

[Application of chromosomal microarray analysis and next-generation sequencing for the analysis of abortic tissues].

Zhao W, Li S, Miao Y, Li J, Yu D. Zhao W, et al. Among authors: yu d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):676-681. doi: 10.3760/cma.j.issn.1003-9406.2019.07.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302909 Chinese.

10

Detection of complex chromosome rearrangements using optical genome mapping.

Qu J, Li S, Yu D. Qu J, et al. Among authors: yu d. Gene. 2023 Oct 30;884:147688. doi: 10.1016/j.gene.2023.147688. Epub 2023 Aug 3. Gene. 2023. PMID: 37543218

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