Fu W - Search Results

1

Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview.

Zhuang J, Chen C, Zhang H, Fu W, Li Y, Jiang Y, Zeng S, Wu X, Xie Y, Wang G. Zhuang J, et al. Among authors: fu w. Mol Cytogenet. 2022 Jul 28;15(1):31. doi: 10.1186/s13039-022-00608-y. Mol Cytogenet. 2022. PMID: 35902965 Free PMC article.

2

Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China.

Zhuang J, Chen C, Jiang Y, Luo Q, Zeng S, Lv C, Wang Y, Fu W. Zhuang J, et al. Among authors: fu w. BMC Pregnancy Childbirth. 2021 Jan 28;21(1):94. doi: 10.1186/s12884-021-03589-9. BMC Pregnancy Childbirth. 2021. PMID: 33509128 Free PMC article.

3

Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array.

Zhuang J, Zhang N, Fu W, Yao J, Li Y, Zeng S, Wang Y, Xie Y, Jiang Y. Zhuang J, et al. Among authors: fu w. Mol Cytogenet. 2021 Sep 29;14(1):46. doi: 10.1186/s13039-021-00568-9. Mol Cytogenet. 2021. PMID: 34587985 Free PMC article.

4

[Non-invasive prenatal testing and genetic diagnosis of a case of Pallister-Killian syndrome].

Wang J, Zhuang J, Jiang Y, Fu W, Wang Y. Wang J, et al. Among authors: fu w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Oct 10;38(10):997-1001. doi: 10.3760/cma.j.cn511374-20201016-00724. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34625941 Chinese.

5

[A case of neonatal Cornelia de Lange syndrome caused by a novel variant of SMC1A gene].

Li Y, Wang Y, Jiang Y, Fu W, Tan M, Zhuang J. Li Y, et al. Among authors: fu w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Nov 10;38(11):1132-1135. doi: 10.3760/cma.j.cn511374-20200530-00400. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34729759 Chinese.

6

Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population.

Zhuang J, Chen C, Fu W, Wang Y, Zhuang Q, Lu Y, Xie T, Xu R, Zeng S, Jiang Y, Xie Y, Wang G. Zhuang J, et al. Among authors: fu w. Arch Pathol Lab Med. 2023 Feb 1;147(2):208-214. doi: 10.5858/arpa.2021-0510-OA. Arch Pathol Lab Med. 2023. PMID: 35639603 Free article.

7

A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures.

Zhuang J, Xie M, Yao J, Fu W, Zeng S, Jiang Y, Wang Y, Xie Y, Wang G, Chen C. Zhuang J, et al. Among authors: fu w. BMC Med Genomics. 2023 Jan 9;16(1):3. doi: 10.1186/s12920-023-01433-x. BMC Med Genomics. 2023. PMID: 36624491 Free PMC article.

8

Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study.

Zhuang J, Zhang N, Fu W, Jiang Y, Chen Y, Chen C. Zhuang J, et al. Among authors: fu w. Mol Cytogenet. 2024 Sep 2;17(1):20. doi: 10.1186/s13039-024-00690-4. Mol Cytogenet. 2024. PMID: 39218907 Free PMC article.

9

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China.

Shi L, Huang H, Jiang Q, Huang R, Fu W, Mao L, Wei X, Cui H, Lin K, Cai L, Yang Y, Wang Y, Wu J. Shi L, et al. Among authors: fu w. Front Genet. 2020 Feb 28;11:130. doi: 10.3389/fgene.2020.00130. eCollection 2020. Front Genet. 2020. PMID: 32184803 Free PMC article.

10

Prognostic Value of Dynamic Measurable Residual Disease Monitoring by Multiflowcytometry in Elderly Patients With Nonintensively Treated Acute Myeloid Leukemia.

Sun Y, Han X, Zhang Y, Fu W, Fang Y, Liu J, Xu L, Wang T, Zhong H. Sun Y, et al. Among authors: fu w. Clin Lymphoma Myeloma Leuk. 2025 Jan 2:S2152-2650(24)02470-4. doi: 10.1016/j.clml.2024.12.020. Online ahead of print. Clin Lymphoma Myeloma Leuk. 2025. PMID: 39863462

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