Cargando…

Editorial: Unravelling the basis of non-invasive prenatal screening results

Detalles Bibliográficos
Autores principales:	De Falco, Luigia, Pelo, Elisabetta, Qi, Zhongxia, Novelli, Antonio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390063/ https://www.ncbi.nlm.nih.gov/pubmed/37529782 http://dx.doi.org/10.3389/fgene.2023.1247764

Ejemplares similares

Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
por: Qi, Zhongxia, et al.
Publicado: (2023)

A retrospective single-center analysis of prenatal diagnosis and follow-up of 626 chinese patients with positive non-invasive prenatal screening results
por: Bu, Xiufen, et al.
Publicado: (2022)

Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis
por: Liu, Sha, et al.
Publicado: (2021)

Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations
por: Wang, Jing, et al.
Publicado: (2021)

Clinical Efficiency of Non-invasive Prenatal Screening for Common Trisomies in Low-Risk and Twin Pregnancies
por: Xu, Yanfei, et al.
Publicado: (2021)

Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis
por: Tang, Xinxin, et al.
Publicado: (2022)

Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China
por: Jing, Xiaosha, et al.
Publicado: (2022)

Cell-Free Fetal Deoxyribonucleic Acid (cffDNA) Analysis as a Remarkable Method of Non-Invasive Prenatal Screening
por: Raj, Himanshu, et al.
Publicado: (2022)

Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing
por: Yu, Jialing, et al.
Publicado: (2022)

Clinical Utility of the Prenatal BACs-on-Beads™ Assay in Invasive Prenatal Diagnosis
por: Jiang, Yu, et al.
Publicado: (2022)

The Clinical Utility of Non-invasive Prenatal Testing for Pregnant Women With Different Diagnostic Indications
por: Zheng, Jianli, et al.
Publicado: (2020)

Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach
por: Alyafee, Yusra, et al.
Publicado: (2022)

Editorial: The Genetic and Environmental Basis for Diseases in Understudied Populations
por: Mulder, Nicola, et al.
Publicado: (2020)

Editorial: Mitochondrial Disorders: Biochemical and Molecular Basis of Disease
por: Leipnitz, Guilhian, et al.
Publicado: (2021)

Editorial: Molecular basis of epigenetic regulation in cancer therapies
por: Carlos-Reyes, Angeles, et al.
Publicado: (2023)

Non-Invasive Prenatal Diagnosis of Monogenic Disorders Through Bayesian- and Haplotype-Based Prediction of Fetal Genotype
por: Li, Jia, et al.
Publicado: (2022)

Non-invasive Prenatal Testing in Pregnancies Following Assisted Reproduction
por: Kamath, Vandana, et al.
Publicado: (2022)

Cases of tetrasomy 9p and trisomy 9p in prenatal diagnosis—Analysis of noninvasive and invasive test results
por: Moczulska, Hanna, et al.
Publicado: (2022)

Editorial: Progress in understanding the immunogenetic basis of disease susceptibility and outcomes
por: Bharani, Tina, et al.
Publicado: (2022)

Case Report: Challenges of Non-Invasive Prenatal Testing (NIPT): A Case Report of Confined Placental Mosaicism and Clinical Considerations
por: Bonanni, Giulia, et al.
Publicado: (2022)

Case Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling
por: Feresin, Agnese, et al.
Publicado: (2022)

Sequencing Shorter cfDNA Fragments Decreases the False Negative Rate of Non-invasive Prenatal Testing
por: Xue, Ying, et al.
Publicado: (2020)

Non-Invasive Prenatal Screening: The First Report of Pentasomy X Detected by Plasma Cell-Free DNA and Karyotype Analysis
por: De Falco, Luigia, et al.
Publicado: (2022)

A Randomized Controlled Trial on the Influence of Prenatal Counseling on the Attitudes and Preferences Toward Invasive Prenatal Testing Among Women in Their First Trimester of Pregnancy (INVASIVE)
por: Paz y Miño, Fernanda, et al.
Publicado: (2020)

Editorial: Advancing our understanding of the genetic and functional basis of skeletal dysplasia
por: Guo, Long, et al.
Publicado: (2023)

Editorial: Molecular dissection of the genetic basis underlying plant complex traits
por: Yang, Yuchen
Publicado: (2023)

Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia
por: Alyafee, Yusra, et al.
Publicado: (2021)

Editorial: Genomic Basis of Developmental Programming in Livestock: Insights Into Nutrition, Health, and Production
por: Diniz, Wellison J. S., et al.
Publicado: (2022)

Non-invasive prenatal testing for the detection of trisomy 13, 18, and 21 and sex chromosome aneuploidies in 68,763 cases
por: Zhang, Yanchun, et al.
Publicado: (2022)

Application of FF-QuantSC for the Precise Estimation of Fetal Fraction in Non-invasive Prenatal Testing in Two SRY-Translocation Cases
por: Zeng, Yan, et al.
Publicado: (2020)

Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?
por: Liehr, Thomas
Publicado: (2021)

Combining Z-Score and Maternal Copy Number Variation Analysis Increases the Positive Rate and Accuracy in Non-Invasive Prenatal Testing
por: Chen, Liheng, et al.
Publicado: (2022)

Clinical interpretation of cell-based non-invasive prenatal testing for monogenic disorders including repeat expansion disorders: potentials and pitfalls
por: Jeppesen, Line Dahl, et al.
Publicado: (2023)

Unraveling Novel Mechanisms of Neurodegeneration Through a Large-Scale Forward Genetic Screen in Drosophila
por: Deal, Samantha L., et al.
Publicado: (2019)

Effectiveness of non-invasive chromosomal screening for normal karyotype and chromosomal rearrangements
por: Sun, Bo-lan, et al.
Publicado: (2023)

Comparison of Efficiencies of Non-invasive Prenatal Testing, Karyotyping, and Chromosomal Micro-Array for Diagnosing Fetal Chromosomal Anomalies in the Second and Third Trimesters
por: Zhu, Yiyang, et al.
Publicado: (2019)

Non-invasive prenatal screening for Emanuel syndrome
por: Luo, Yuqin, et al.
Publicado: (2020)

Non-invasive prenatal testing can detect silent cancers in expecting mothers
por: Ottaiano, Alessandro, et al.
Publicado: (2023)

Assessment of a change of protocol of prenatal screening by inclusion of non-invasive prenatal diagnosis
por: Cabra-Rodríguez, Rocío, et al.
Publicado: (2020)

Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases
por: Zhang, Yan, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_jo109taiba1tpe6vm3fo0fn5j6