Zou Y - Search Results

1

[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with N-acetylglutamate synthase deficiency].

Chen J, Yuan H, Xie K, Guo Z, Yang Y, Zou Y, Chen G, Liu Y. Chen J, et al. Among authors: zou y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Dec 10;37(12):1360-1363. doi: 10.3760/cma.j.cn511374-20200203-00055. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33306822 Chinese.

2

[Study of the phenylalanine hydroxylase gene variants in patients with phenylketonuria from Jiangxi province].

Lu Q, Liu Y, Yang B, Xie K, Zou Y, Lu W, Wang F. Lu Q, et al. Among authors: zou y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1057-1061. doi: 10.3760/cma.j.issn.1003-9406.2019.11.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703125 Chinese.

3

A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family.

Luo H, Zou Y, Liu Y. Luo H, et al. Among authors: zou y. Hemoglobin. 2020 Jan;44(1):55-57. doi: 10.1080/03630269.2020.1714648. Epub 2020 Jan 15. Hemoglobin. 2020. PMID: 31939318

4

A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family.

Chen J, Yuan H, Xie K, Wang X, Tan L, Zou Y, Yang Y, Pan L, Xiao J, Chen G, Liu Y. Chen J, et al. Among authors: zou y. BMC Cardiovasc Disord. 2020 Jan 20;20(1):27. doi: 10.1186/s12872-019-01322-1. BMC Cardiovasc Disord. 2020. PMID: 31959127 Free PMC article.

5

[Prenatal diagnosis of a fetus with 8q13.3 microdeletion through chromosomal microarray analysis].

Rao H, Liu Y, Xiao J, Zou Y, Yuan H. Rao H, et al. Among authors: zou y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Mar 10;38(3):268-270. doi: 10.3760/cma.j.cn511374-20200217-00086. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33751539 Chinese.

6

Wooden-Tip Electrospray Mass Spectrometry Characterization of Human Hemoglobin in Whole Blood Sample for Thalassemia Screening: A Pilot Study.

Huang T, Huang T, Zou Y, Xie K, Shen Y, Zhang W, Huang S, Liu Y, Yang B. Huang T, et al. Among authors: zou y. Molecules. 2022 Jun 20;27(12):3952. doi: 10.3390/molecules27123952. Molecules. 2022. PMID: 35745074 Free PMC article.

7

Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy.

Zou Y, Luo H, Yuan H, Xie K, Yang Y, Huang S, Yang B, Liu Y. Zou Y, et al. Front Neurol. 2022 Jul 6;13:904027. doi: 10.3389/fneur.2022.904027. eCollection 2022. Front Neurol. 2022. PMID: 35873758 Free PMC article.

8

Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.

Luo H, Huang T, Lu Q, Zhang L, Xu Y, Yang Y, Guo Z, Yuan H, Shen Y, Huang S, Yang B, Zou Y, Liu Y. Luo H, et al. Among authors: zou y. Front Genet. 2022 Sep 28;13:992073. doi: 10.3389/fgene.2022.992073. eCollection 2022. Front Genet. 2022. PMID: 36246595 Free PMC article.

9

In Vitro Inhibitory Effects of Maqian Essential Oil against Ectopic Endometrial Stromal Cells and LPS-Induced Endometrial Epithelial Cells.

Li LP, Luo Y, Huang C, Wang XR, Huang TT, Zou YY, Huang SH, Liu YQ, Yang BC. Li LP, et al. Among authors: zou yy. Chem Biodivers. 2022 Dec;19(12):e202200756. doi: 10.1002/cbdv.202200756. Epub 2022 Dec 3. Chem Biodivers. 2022. PMID: 36377549

10

Concurrent newborn hearing and genetic screening of common hearing loss variants with bloodspot-based targeted next generation sequencing in Jiangxi province.

Luo H, Yang Y, Wang X, Xu F, Huang C, Liu D, Zhang L, Huang T, Ma P, Lu Q, Huang S, Yang B, Zou Y, Liu Y. Luo H, et al. Among authors: zou y. Front Pediatr. 2022 Oct 31;10:1020519. doi: 10.3389/fped.2022.1020519. eCollection 2022. Front Pediatr. 2022. PMID: 36389375 Free PMC article.

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