Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
about
Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnosticsRecent advances in prenatal genetic screening and testingDynamics and ethics of comprehensive preimplantation genetic testing: a review of the challengesWhole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing.Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and familiesA qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.Defining and managing incidental findings in genetic and genomic practice.Genomic futures of prenatal screening: ethical reflection.Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.Call for prudence in whole-genome testing.Three clinical experiences with SNP array results consistent with parental incest: a narrative with lessons learned.A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases.Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?Advantages of expanded universal carrier screening: what is at stake?NIPT-based screening for Down syndrome and beyond: what do pregnant women think?The introduction of arrays in prenatal diagnosis: a special challenge.Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.Current controversies in prenatal diagnosis 2: should incidental findings arising from prenatal testing always be reported to patients?Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testingThe use of arrays to detect copy-number variations in clinical practice
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Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
description
im Juni 2012 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2012
@uk
name
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@en
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@nl
type
label
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@en
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@nl
prefLabel
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@en
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@nl
P2093
P2860
P356
P1433
P1476
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
@en
P2093
Birgit Sikkema-Raddatz
Christine de Die-Smulders
Guido de Wert
Wybo Dondorp
P2860
P304
P356
10.1002/HUMU.22068
P407
P577
2012-06-01T00:00:00Z