Works matching DE "PRENATAL genetic testing"
Results: 490
Genetic Testing, Birth, and the Quest for Health.
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- Science, Technology & Human Values, 2014, v. 39, n. 3, p. 374, doi. 10.1177/0162243913509413
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- Article
Informing policy for the Australian context – Costs, outcomes and cost savings of prenatal carrier screening for cystic fibrosis.
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- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2010, v. 50, n. 1, p. 51, doi. 10.1111/j.1479-828X.2009.01111.x
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- Article
Are pregnant Australian women well informed about prenatal genetic screening? A systematic investigation using the Multidimensional Measure of Informed Choice.
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- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2006, v. 46, n. 5, p. 433, doi. 10.1111/j.1479-828X.2006.00630.x
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- Article
AUTONOMÍA DE LA VOLUNTAD Y SELECCIÓN EMBRIONARIA EN EL MARCO DE LAS TÉCNICAS DE REPRODUCCIÓN ASISTIDA.
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- Revista Jurídica de la Universidad Autonóma de Madrid, 2018, n. 38, p. 317, doi. 10.15366/rjuam2018.38.011
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- Article
Response to Correspondence by Piacentini et al.
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- Pediatric Cardiology, 2024, v. 45, n. 2, p. 455, doi. 10.1007/s00246-023-03369-6
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- Article
The Evaluation of Fetal Cardiac Remote Screening in the Second Trimester of Pregnancy Using the Spatio-Temporal Image Correlation Method.
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- Pediatric Cardiology, 2020, v. 41, n. 5, p. 979, doi. 10.1007/s00246-020-02346-7
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- Article
The impact of third-trimester genetic counseling.
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- 2018
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- Publication type:
- journal article
Prenatal-screening companies expand scope of DNA tests.
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- Nature, 2014, v. 507, n. 7490, p. 19, doi. 10.1038/507019a
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- Article
Genetic tests: Politics and fetal diagnostics collide.
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- Nature, 2012, v. 491, n. 7422, p. 33, doi. 10.1038/491033a
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- Article
Non-invasive prenatal measurement of the fetal genome.
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- Nature, 2012, v. 487, n. 7407, p. 320, doi. 10.1038/nature11251
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- Article
Internet-Based Abnormal Chromosomal Diagnosis During Pregnancy Using a Noninvasive Innovative Approach to Detecting Chromosomal Abnormalities in the Fetus: Scoping Review.
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- JMIR Bioinformatics & Biotechnology, 2024, v. 5, n. 1, p. 1, doi. 10.2196/58439
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- Article
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 4, p. 1775, doi. 10.3906/sag-2006-103
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- Article
Is the management of Rh-Rh incompatibility with noninvasive fetal Rh genotyping for targeted prophylaxis cost-effective in the Turkish population?
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- Turkish Journal of Medical Sciences, 2018, v. 48, n. 1, p. 1, doi. 10.3906/sag-1511-87
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- Article
Genetic carrier screening in pregnancy Informing patients.
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- Medicine Today, 2023, v. 24, n. 3, p. 39
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- Article
Non-Invasive Testing, Non-Invasive Counseling.
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- Journal of Law, Medicine & Ethics, 2015, v. 43, n. 2, p. 228, doi. 10.1111/jlme.12237
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- Article
Reproductive Information and Reproductive Decision-Making.
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- Journal of Law, Medicine & Ethics, 2015, v. 43, n. 2, p. 241, doi. 10.1111/jlme.12238
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- Article
Another Strike Against Eugenic Abortion.
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- Human Life Review, 2021, v. 47, n. 4, p. 49
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- Article
An Evening with Sarah.
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- Human Life Review, 2019, v. 45, n. 1, p. 85
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- Article
Eugenics Triumphant in Prenatal Testing.
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- Human Life Review, 2009, v. 35, n. 4, p. 87
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- Article
孕中期超声联合无创产前基因筛查在检出染色体异常胎儿中的应用价值.
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- Progress in Modern Biomedicine, 2023, v. 23, n. 17, p. 3382, doi. 10.13241/j.cnki.pmb.2023.17.035
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- Article
Current practice and future perspective of the Prenatal Genetic Service in Slovenia.
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- Paediatria Croatica, 2015, v. 59, n. 2, p. 106, doi. 10.13112/PC.2015.17
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- Article
Mortality in Neonatal Intensive Care Units in Iran: A Systematic Review and Meta-Analysis.
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- Iranian Journal of Neonatology, 2019, v. 10, n. 3, p. 70, doi. 10.22038/ijn.2019.36647.1566
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- Article
Advancing prenatal diagnosis through comprehensive fetal cell‐free DNA screening.
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- Clinical & Translational Medicine, 2024, v. 14, n. 12, p. 1, doi. 10.1002/ctm2.70129
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- Article
A new strategy for prenatal genetic screening of copy number variations in the DMD gene: A large cohort study based on NIPT analysis.
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- Clinical & Translational Medicine, 2024, v. 14, n. 5, p. 1, doi. 10.1002/ctm2.1706
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- Article
Targeted Sequencing and RNA Assay Reveal a Noncanonical JAG1 Splicing Variant Causing Alagille Syndrome.
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- Frontiers in Genetics, 2020, v. 10, p. 1, doi. 10.3389/fgene.2019.01363
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- Article
Using Comparison Scenarios to Improve Prenatal Risk Communication.
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- 2013
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- Journal Article
Testing Times Ahead: Non‐Invasive Prenatal Testing and the Kind of Community We Want to Be.
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- Modern Law Review, 2018, v. 81, n. 4, p. 646, doi. 10.1111/1468-2230.12355
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- Article
Expert Knowledge Influences Decision-Making for Couples Receiving Positive Prenatal Chromosomal Microarray Testing Results.
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- 2017
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- journal article
Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6).
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- American Journal of Case Reports, 2022, v. 23, p. 2, doi. 10.12659/AJCR.935370
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- Article
Hereditary Neuromuscular Disorders in Reproductive Medicine.
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- Genes, 2024, v. 15, n. 11, p. 1409, doi. 10.3390/genes15111409
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- Article
Non-Invasive Prenatal Screening from a Genetic Counseling Prospective: Pre and Post-Genetic Counseling Regarding Rare Chromosomal Abnormalities and Incidental Finding.
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- Genes, 2024, v. 15, n. 10, p. 1349, doi. 10.3390/genes15101349
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- Article
Early Non-Invasive Prenatal Testing at 6–9 Weeks of Gestation.
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- Genes, 2024, v. 15, n. 7, p. 895, doi. 10.3390/genes15070895
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- Article
A Case Report of a Feto-Placental Mosaicism Involving a Segmental Aneuploidy: A Challenge for Genome Wide Screening by Non-Invasive Prenatal Testing of Cell-Free DNA in Maternal Plasma.
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- 2023
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- Publication type:
- Case Study
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis.
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- Genes, 2023, v. 14, n. 3, p. 563, doi. 10.3390/genes14030563
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- Article
Prenatal Genetic Testing in the Era of Next Generation Sequencing: A One-Center Canadian Experience.
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- Genes, 2022, v. 13, n. 11, p. 2019, doi. 10.3390/genes13112019
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- Article
Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation.
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- Genes, 2022, v. 13, n. 9, p. 1517, doi. 10.3390/genes13091517
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- Article
Optical Genome Mapping as a Next-Generation Cytogenomic Tool for Detection of Structural and Copy Number Variations for Prenatal Genomic Analyses.
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- Genes, 2021, v. 12, n. 3, p. 398, doi. 10.3390/genes12030398
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- Article
The Pregnancy Outcome of Mosaic Embryo Transfer: A Prospective Multicenter Study and Meta-Analysis.
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- Genes, 2020, v. 11, n. 9, p. 973, doi. 10.3390/genes11090973
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- Article
Non-invasive prenatal testing: a review of international implementation and challenges.
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- International Journal of Women's Health, 2015, v. 7, p. 113, doi. 10.2147/IJWH.S67124
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- Article
She Has Her Mother's Laugh: The Powers, Perversions, and Potential of Heredity.
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- Journal of the Association of Genetic Technologists, 2019, v. 45, n. 2, p. 81
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- Article
Novel Application of HDlive Silhouette and HDliveFlow: Clinical Significance of the 'See-through Fashion' in Prenatal Diagnosis.
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- Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2016, v. 10, n. 1, p. 90, doi. 10.5005/jp-journals-10009-1447
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- Article
Patient Decision Aids for Prenatal Genetic Testing: Probability, Embodiment, and Problematic Integration.
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- Health Communication, 2017, v. 32, n. 5, p. 568, doi. 10.1080/10410236.2016.1140500
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- Article
Indications, types, and diagnostic implications of prenatal genetic testing in Sub-Saharan Africa: A descriptive study.
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- PLoS ONE, 2023, v. 18, n. 11, p. 1, doi. 10.1371/journal.pone.0294409
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- Article
Biobanks: Challenges for ‘ethics’.
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- 2005
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- Publication type:
- Editorial
The SafeBirth Clinic.
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- INFORMS Transactions on Education, 2021, v. 22, n. 1, p. 148, doi. 10.1287/ited.2019.0241cs
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- Article
Prenatal karyotype results from 2169 invasive tests.
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- Ginekologia Polska, 2023, v. 94, n. 11, p. 1, doi. 10.5603/GP.a2022.0143
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- Publication type:
- Article
Increased risk of low infant birth weight in pregnant women with low PAPP-A values measured in the first trimester.
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- Ginekologia Polska, 2023, v. 94, n. 9, p. 714, doi. 10.5603/GP.a2022.0118
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- Article
Strategies to improve early diagnosis of Klinefelter syndrome.
- Published in:
- 2020
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- Publication type:
- Editorial
Identification of MicroRNA Profiles in Fetal Spina Bifida: The Role in Pathomechanism and Diagnostic Significance.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 5, p. 2896, doi. 10.3390/ijms25052896
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- Publication type:
- Article
Genome-Wide Copy Number Variant and High-Throughput Transcriptomics Analyses of Placental Tissues Underscore Persisting Child Susceptibility in At-Risk Pregnancies Cleared in Standard Genetic Testing.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11448, doi. 10.3390/ijms231911448
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- Publication type:
- Article