The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences. - Wikidata - wikimedia - TriplyDB

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.

http://www.wikidata.org/entity/Q37421257

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Association between EN1 rs4144782 and susceptibility of knee osteoarthritis: A case-control study.Prenatal ultrasound parameters in single-suture craniosynostosis.Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases.The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations.Advanced genomic testing may aid in counseling of isolated agenesis of the corpus callosum on prenatal ultrasound.Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?

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The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.

http://www.wikidata.org/entity/Q37421257

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bilimsel makale

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scientific article published on 25 May 2016

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vedecký článok

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vetenskaplig artikel

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The Psychological Impact of Pr ...... sions of Parents' Experiences.

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S10897-016-9960-Y

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Journal of Genetic Counseling

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D Van Opstal

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J Verhagen-Visser

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K E M Diderich

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L C P Govaerts

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M F C M Knapen

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M Joosten

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R J H Galjaard

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S L van der Steen

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S R Riedijk

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P2860

The law of incidental findings in human subjects research: establishing researchers' duties

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.

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The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.

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1227-1234

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10.1007/S10897-016-9960-Y

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6

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Malgorzata Srebniak

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