Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing. - Wikidata - wikimedia - TriplyDB

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.

http://www.wikidata.org/entity/Q34433169

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Recent advances in prenatal genetic screening and testing Repeated failed non-invasive prenatal testing in a woman with immune thrombocytopenia and antiphospholipid syndrome: lessons learnt.Non-invasive prenatal testing for sex chromosome abnormalities: a source of confusion Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral center An Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population.Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18.Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS)Noninvasive prenatal testing in the general obstetric population: clinical performance and counseling considerations in over 85 000 cases.Non-invasive Prenatal Testing (NIPT): Better Meet an Expert!: The Case of a Late Detected Trisomy 13 Reveals Structural Problems in NIPT Counselling and Highlights Substantial Risks for the Reproductive Autonomy.Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage.Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.Single Nucleotide Polymorphism-Based Analysis of Cell-Free Fetal DNA in 3000 Cases from Germany and Austria Report on noninvasive prenatal testing: classical and alternative approaches.Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles.NIPTRIC: an online tool for clinical interpretation of non-invasive prenatal testing (NIPT) results.Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage.Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.Clinical implementation of NIPT - technical and biological challenges.Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNA How to perform transabdominal chorionic villus sampling: a practical guideline.Current status of non-invasive prenatal testing in Japan.The implications of non-invasive prenatal testing failures: a review of an under-discussed phenomenon.Fetal aneuploidy screening with cell-free DNA in late gestation.Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods.Cell-Free DNA Screening: Complexities and Challenges of Clinical Implementation.The IONA® Test: Development of an Automated Cell-Free DNA-Based Screening Test for Fetal Trisomies 13, 18, and 21 That Employs the Ion Proton Semiconductor Sequencing Platform.Discordant non-invasive prenatal testing (NIPT) - a systematic review.Lost in Translation? Ethical Challenges of Implementing a New Diagnostic Procedure.Clinical, social and ethical issues associated with non-invasive prenatal testing for aneuploidy.Validation of combinatorial probe-anchor ligation-based sequencing as non-invasive prenatal test for trisomy at a central laboratory.Effects of Maternal and Fetal Characteristics on Cell-Free Fetal DNA Fraction in Maternal Plasma.Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.Impact of the increased adoption of prenatal cfDNA screening on non-profit patient advocacy organizations in the United States.Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG).Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.

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P2860

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.

http://www.wikidata.org/entity/Q34433169

description

2014 nî lūn-bûn

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2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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J.AJOG.2014.08.006

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American Journal of Obstetrics and Gynecology

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Clinical experience and follow ...... e prenatal aneuploidy testing.

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Allison Ryan

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Bernhard Zimmermann

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Charles M Strom

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Kirsten J Curnow

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10.1016/J.AJOG.2014.08.006

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single-nucleotide polymorphism