Cargando…

Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China

Non-invasive prenatal testing (NIPT) is an incomparable prenatal screening technology, but we should undergo amniocentesis to confirm fetal chromosome when pregnancies receive a positive result via NIPT. We aimed to investigate the detection rate and positive predictive value of NIPT results in preg...

Descripción completa

Detalles Bibliográficos
Autores principales:	Dai, Rulin, Yu, Yang, Zhang, Han, Li, Leilei, Jiang, Yuting, Liu, Ruizhi, Zhang, Hongguo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2021
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545248/ https://www.ncbi.nlm.nih.gov/pubmed/33578623 http://dx.doi.org/10.1097/MD.0000000000024740

Ejemplares similares

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

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

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)

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)

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)

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

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

Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient: A case report
por: He, Jing, et al.
Publicado: (2020)

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

Molecular diagnosis of sex chromosome mosaics in fetal amniotic cells
por: Fan, Zuqian, et al.
Publicado: (2021)

A novel FGFR2 (S137W) mutation resulting in Apert syndrome: A case report
por: Shi, Qingyang, et al.
Publicado: (2020)

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

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

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

Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing
por: Gu, Xiaoyan, et al.
Publicado: (2018)

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

Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports
por: Wang, Li, et al.
Publicado: (2022)

Common variants in IL-17A/IL-17RA axis contribute to predisposition to and progression of congestive heart failure
por: Sandip, Chaugai, et al.
Publicado: (2016)

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

Fetal cardiac rhabdomyoma due to paternal mosaicism of TSC2: A case report
por: Chen, Lin, et al.
Publicado: (2020)

Noninvasive prenatal testing in routine clinical practice for a high-risk population: Experience from a center
por: Qi, Guijie, et al.
Publicado: (2016)

Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China
por: Dai, Rulin, et al.
Publicado: (2019)

The genotype and phenotype of chromosome 18p deletion syndrome: Case series
por: Jin, Qiujie, et al.
Publicado: (2021)

A novel F8 variant in a Chinese hemophilia A family and involvement of X-chromosome inactivation: A case report
por: Zhang, Honghong, et al.
Publicado: (2023)

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)

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

Co-existence of well-differentiated fetal adenocarcinoma of the lung with tuberculosis in a young female: A rare case report
por: Guo, Fengzhu, et al.
Publicado: (2019)

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)

Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature
por: Li, Linlin, et al.
Publicado: (2020)

Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary Lesions: An Observational Study
por: Lee, I-Te, et al.
Publicado: (2015)

A boy with 13.34-Mb interstitial deletion of chromosome 4p15: A new case report and review of the literature
por: Mitroi, Anca Florentina, et al.
Publicado: (2017)

Familial chylomicronemia syndrome due to a heterozygous deletion of the chromosome 8 treated with the apoCIII inhibitor volanesorsen: A case report
por: Tünnemann-Tarr, Adrienn, et al.
Publicado: (2021)

Evolution of the search for a common mechanism of congenital risk of coronary heart disease and type 2 diabetes mellitus in the chromosomal locus 9p21.3
por: Benberin, Valeriy, et al.
Publicado: (2023)

Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: A case report
por: Aleksiūnienė, Beata, et al.
Publicado: (2017)

Coexistence of t(2;14;11)(p16.1;q32;q23) and t(14;19)(q32;q13.3) chromosome translocations in a patient with chronic lymphocytic leukemia: A case report
por: Liu, Guangming, et al.
Publicado: (2017)

Effect of multiple clinical factors on recurrent angina after percutaneous coronary intervention: A retrospective study from 398 ST-segment elevation myocardial infarction patients
por: Zhang, Jing, et al.
Publicado: (2016)

Association between interleukin-6 gene polymorphisms and febrile seizure risk: A meta-analysis
por: Chen, Qingling, et al.
Publicado: (2019)

A Causal Role of Genetically Elevated Circulating Interleukin-10 in the Development of Digestive Cancers: Evidence from Mendelian Randomization Analysis Based on 29,307 Subjects
por: Niu, Wenquan, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_5rg4u9a486j7anekq6a0p2jilk