Zhang Q - Search Results

1

New Ratios for Performance Improvement for Identifying Acyl-CoA Dehydrogenase Deficiencies in Expanded Newborn Screening: A Retrospective Study.

Wang B, Zhang Q, Gao A, Wang Q, Ma J, Li H, Wang T. Wang B, et al. Among authors: zhang q. Front Genet. 2019 Sep 18;10:811. doi: 10.3389/fgene.2019.00811. eCollection 2019. Front Genet. 2019. PMID: 31620161 Free PMC article.

2

Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population.

Wang T, Ma J, Zhang Q, Gao A, Wang Q, Li H, Xiang J, Wang B. Wang T, et al. Among authors: zhang q. Front Genet. 2019 Oct 29;10:1052. doi: 10.3389/fgene.2019.01052. eCollection 2019. Front Genet. 2019. PMID: 31737040 Free PMC article.

3

Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia.

Tang H, Zhang Q, Xiang J, Yin L, Wang J, Wang T. Tang H, et al. Among authors: zhang q. Front Genet. 2021 Mar 10;12:599863. doi: 10.3389/fgene.2021.599863. eCollection 2021. Front Genet. 2021. PMID: 33777089 Free PMC article.

4

Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing.

Xiang J, Ding Y, Yang F, Gao A, Zhang W, Tang H, Mao J, He Q, Zhang Q, Wang T. Xiang J, et al. Among authors: zhang q, zhang w. Front Genet. 2021 Nov 10;12:738561. doi: 10.3389/fgene.2021.738561. eCollection 2021. Front Genet. 2021. PMID: 34858471 Free PMC article.

5

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies.

Xiang J, Ding Y, Song X, Mao J, Liu M, Liu Y, Huang C, Zhang Q, Wang T. Xiang J, et al. Among authors: zhang q. Front Genet. 2020 Nov 6;11:571219. doi: 10.3389/fgene.2020.571219. eCollection 2020. Front Genet. 2020. PMID: 33240322 Free PMC article.

6

Investigating the Metabolic Model in Preterm Neonates by Tandem Mass Spectrometry: A Cohort Study.

Wang B, Zhang Q, Wang Q, Ma J, Cao X, Chen Y, Pan Y, Li H, Xiang J, Wang T. Wang B, et al. Among authors: zhang q. Horm Metab Res. 2021 Feb;53(2):112-123. doi: 10.1055/a-1300-2294. Epub 2020 Nov 27. Horm Metab Res. 2021. PMID: 33246344

7

[A novel mutation in the ETFDH gene of an infant with multiple acyl-CoA dehydrogenase deficiency].

Gao A, Qiao LW, Duan CY, Zhao NN, Zhang W, Zhang Q. Gao A, et al. Among authors: zhang q, zhang w. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Jul;20(7):529-533. doi: 10.7499/j.issn.1008-8830.2018.07.003. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 30022752 Free PMC article. Chinese.

8

Correction: Investigating the Metabolic Model in Preterm Neonates by Tandem Mass Spectrometry: A Cohort Study.

Wang B, Zhang Q, Wang Q, Ma J, Cao X, Chen Y, Pan Y, Li H, Xiang J, Wang T. Wang B, et al. Among authors: zhang q. Horm Metab Res. 2021 Feb;53(2):e1. doi: 10.1055/a-1325-3731. Epub 2020 Dec 10. Horm Metab Res. 2021. PMID: 33302317 No abstract available.

9

Noninvasive Prenatal Screening for Fetal Sex Chromosome Aneuploidies at Two Next-Generation Sequencing Platforms.

Xue Y, Li H, Zhang Q, Zhao G, Ding J, Shen C, Qiao L, Wang T. Xue Y, et al. Among authors: zhang q. Ann Clin Lab Sci. 2018 Jul;48(4):501-505. Ann Clin Lab Sci. 2018. PMID: 30143493

10

[Identification of a novel NF1 mutation in a Chinese family affected with neurofibromatosis type I].

Zhang Q, Liang Y, Gao A, Duan C, Ding Y, Pan Y, Qiao L, Li H. Zhang Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Feb 10;36(2):132-135. doi: 10.3760/cma.j.issn.1003-9406.2019.02.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30703230 Chinese.

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