Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y. - Test2 - elhamkhani - TriplyDB

Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

http://www.wikidata.org/entity/Q38860845

about

Reconciling evidence-based medicine and precision medicine in the era of big data: challenges and opportunities The importance of copy number variation in congenital heart disease False negative fetal cell free DNA screening for microdeletion syndromes in the presence of an unbalanced translocation involving monosomy 4p.Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis.Attitudes towards non-invasive prenatal diagnosis among obstetricians in Pakistan, a developing, Islamic country.Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.Comment on "The clinical utility of genome-wide non invasive prenatal screening".Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations.Recent developments in genetics and medically assisted reproduction: from research to clinical applications

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P2860

Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

http://www.wikidata.org/entity/Q38860845

description

2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

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Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

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Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

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Clinical Genetics

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Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.

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P2860

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics

Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing.

Association of copy number variants with specific ultrasonographically detected fetal anomalies

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.

Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.

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

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477-485

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scholarly article

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10.1111/CGE.12818

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6

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90

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2016-06-10T00:00:00Z

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27283893

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