Cargando…

Noninvasive prenatal testing in routine clinical practice for a high-risk population: Experience from a center

This study aimed to summarize the effects of noninvasive prenatal testing (NIPT) on aneuploidy among high-risk participants in Tangshan Maternal and Children Health Hospital. NIPT or invasive prenatal diagnosis was recommended to patients with a high risk of fetal aneuploidy from February 2013 to Fe...

Descripción completa

Detalles Bibliográficos
Autores principales:	Qi, Guijie, Yi, Jianping, Han, Baosheng, Liu, Heng, Guo, Wanru, Shi, Chong, Yin, Lirong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2016
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072963/ https://www.ncbi.nlm.nih.gov/pubmed/27741136 http://dx.doi.org/10.1097/MD.0000000000005126

Ejemplares similares

Preimplantation genetic testing and prenatal diagnosis in a family with pseudovaginal perineoscrotal hypospadias: A case report
por: Chen, Jiayao, et al.
Publicado: (2023)

Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China
por: Dai, Rulin, et al.
Publicado: (2021)

Missed diagnosis of lissencephaly after prenatal diagnosis: A case report
por: Liu, Mengna, et al.
Publicado: (2023)

Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review
por: Yue, Fagui, et al.
Publicado: (2021)

Prenatal diagnosis of 7q11.23 microdeletion: Two cases report and literature review
por: Lv, Xin, et al.
Publicado: (2023)

Prenatal diagnosis and genetic analysis of a fetus with Branchio-oto-renal syndrome: A case report
por: Tang, Ping, et al.
Publicado: (2022)

Prenatal diagnosis of chromosome 18 long arm deletion syndrome by high-throughput sequencing: Two case reports
por: Bai, Xuechun, et al.
Publicado: (2021)

Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2021)

Identification of a rare missense mutation in GJB1 and prenatal diagnosis in a Chinese family with CMT: A case report
por: Huang, Xinyi, et al.
Publicado: (2022)

Prenatal detection of a 7q11.21 microdeletion (517–605 kb): A variant with normal characteristics at birth (STROBE)
por: Zhang, Hongguo, et al.
Publicado: (2021)

Prenatal detection of pure proximal 6q14.1 microduplication encompassing LCA5 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2022)

Prenatal detection of distal 1q21.1q21.2 microduplication with abnormal ultrasound findings: Two cases report and literature review
por: Zhang, Hongguo, et al.
Publicado: (2021)

A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report
por: Sha, Jing, et al.
Publicado: (2022)

The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study
por: Zhang, Yinhong, et al.
Publicado: (2020)

Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency: A case report and literature review
por: Sun, Meiling, et al.
Publicado: (2020)

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study
por: Cai, Meiying, et al.
Publicado: (2022)

Pulmonary and mediastinum metastasis of uterine leiomyoma: A case report
por: Huang, Liqiang, et al.
Publicado: (2019)

Multiple adverse drug reactions and genetic polymorphism testing: A case report with negative result
por: Arellano, Ana Lucía, et al.
Publicado: (2017)

The relationship between RASSF1A promoter methylation and thyroid carcinoma: A meta-analysis of 14 articles and a bioinformatics of 2 databases (PRISMA)
por: Niu, Heng, et al.
Publicado: (2017)

Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
por: Hu, Hua, et al.
Publicado: (2021)

Effects of individualized administration of folic acid on prothrombotic state and vascular endothelial function with H-type hypertension: A double-blinded, randomized clinical cohort study
por: Zhang, Song, et al.
Publicado: (2022)

NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literature
por: Shi, Chuan, et al.
Publicado: (2016)

The effects of NLRP3 and MAVS gene polymorphisms on the risk of asthma: A case–control study
por: Xulong, Cai, et al.
Publicado: (2022)

Prognostic significance of long intergenic non-protein-coding RNA 511expression in malignant tumors: A systematic review and meta-analysis
por: Chen, Ming, et al.
Publicado: (2020)

Comprehensive analyses of potential key genes in active tuberculosis: A systematic review
por: Chen, Jiarui, et al.
Publicado: (2021)

Novel chromosomal microduplications associated with dolichocephaly craniosynostosis: A case report
por: Yu, Dongyi, et al.
Publicado: (2017)

Expression patterns and prognostic value of m(6)A RNA methylation regulators in adrenocortical carcinoma
por: Fu, Yang, et al.
Publicado: (2021)

Identification of hub genes, key pathways, and therapeutic agents in Hutchinson–Gilford Progeria syndrome using bioinformatics analysis
por: Wang, Dengchuan, et al.
Publicado: (2020)

Clinicopathological and prognostic significance of NM23 expression in patients with non-small cell lung cancer: A systematic review and meta-analysis
por: Min, Shi-hui, et al.
Publicado: (2021)

Microarray profiling of circular RNAs in steroid-associated osteonecrosis of the femoral head: Observational study
por: Yao, Tao, et al.
Publicado: (2020)

Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome: A case report
por: Shi, Huijun, et al.
Publicado: (2021)

Role of microRNA-130a in the pathogeneses of obstructive sleep apnea hypopnea syndrome-associated pulmonary hypertension by targeting the GAX gene
por: An, Zhe, et al.
Publicado: (2017)

Network and pathway-based analyses of genes associated with osteoporosis
por: Gu, Huijie, et al.
Publicado: (2020)

Association between CYP2B6 c.516G >T variant and acute leukaemia: A protocol for systematic review and meta-analysis
por: Xiong, Xuan, et al.
Publicado: (2021)

Molecular characterization of small supernumerary marker chromosomes derived from chromosome 14/22 detected in adult women with fertility problems: Three case reports and literature review
por: Sun, Meiling, et al.
Publicado: (2020)

Case report: A non-obstructive azoospermia patient with heat shock factor-2 mutation
por: Zhao, Haiyue, et al.
Publicado: (2020)

Chromosomal copy number variations in products of conception from spontaneous abortion by next-generation sequencing technology
por: Dai, Rulin, et al.
Publicado: (2019)

HLA-A and HLA-B genes are involved in the pathogenesis of IBS
por: Liang, Huiping, et al.
Publicado: (2023)

A DNA methylation-associated nomogram predicts the overall survival of osteosarcoma
por: Shi, Jun, et al.
Publicado: (2020)

Association between IL-1β polymorphisms and gastritis risk: A meta-analysis
por: Sun, Xiaoming, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_kd2vqb9mb48ie8h9or811e96d5