Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis.
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Recent advances in prenatal genetic screening and testingPrevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnanciesEffect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trialPopulation-based trends in prenatal screening and diagnosis for aneuploidy: a retrospective analysis of 38 years of state-wide data.Utility of ultrasound examination at 10-14 weeks prior to cell-free DNA screening for fetal aneuploidy.Association of copy number variants with specific ultrasonographically detected fetal anomaliesPrenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma.Analyzing the most frequent disease loci in targeted patient categories optimizes disease gene identification and test accuracy worldwide.Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong KongPrenatal screening of cytogenetic anomalies - a Western Indian experienceCounseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis.Exome Sequencing in Fetuses with Structural MalformationsPaired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural VariationCopy number variants, aneuploidies, and human diseaseA genome-wide screen for copy number alterations in an adolescent pilot cohort with müllerian anomalies.Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations.Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNALimited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.Genetic counseling for men with recurrent pregnancy loss or recurrent implantation failure due to abnormal sperm chromosomal aneuploidyPrenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.A single center's experience with noninvasive prenatal testing.Prenatal diagnosis of chromosomal imbalances.Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypes.An update on current prenatal testing options: first trimester and noninvasive prenatal testing.Genomic futures of prenatal screening: ethical reflection.Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.Comprehensive Review of the Stillborn Placenta.Cell-Free DNA Screening: Complexities and Challenges of Clinical Implementation.Twin pregnancy complicated by esophageal atresia, duodenal atresia, gastric perforation, and hypoplastic left heart structures in one twin: a case report and review of the literaturePreferences for results from genomic microarrays: comparing parents and health care providers.Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis.Pregnant patients' risk perception of prenatal test results with uncertain fetal clinical significance: ultrasound versus advanced genetic testing.Characteristics of rare and private deletions identified in phenotypically normal individuals."Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.
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Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis.
description
2013 nî lūn-bûn
@nan
2013年の論文
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2013年学术文章
@wuu
2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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name
Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
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Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
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type
label
Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
@en
Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
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Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
@en
Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
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P1476
Committee Opinion No. 581: the ...... nalysis in prenatal diagnosis.
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P2093
American College of Obstetricians and Gynecologists Committee on Genetics
P304
P356
10.1097/01.AOG.0000438962.16108.D1
P407
P577
2013-12-01T00:00:00Z