Found: 21
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The accuracy of cell‐free DNA screening for fetal segmental copy number variants: A systematic review and meta‐analysis.
- Published in:
- BJOG: An International Journal of Obstetrics & Gynaecology, 2023, v. 130, n. 6, p. 549, doi. 10.1111/1471-0528.17386
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- Publication type:
- Article
'Taking Its Toll': The Challenges of Working in Fetal Medicine.
- Published in:
- Birth: Issues in Perinatal Care, 2013, v. 40, n. 1, p. 52, doi. 10.1111/birt.12029
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- Publication type:
- Article
Early Diagnosis and Differences in Progression of Fetal Encephalocele.
- Published in:
- Journal of Ultrasound in Medicine, 2020, v. 39, n. 7, p. 1435, doi. 10.1002/jum.15217
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- Publication type:
- Article
Experiences of receiving an increased chance of sex chromosome aneuploidy result from non‐invasive prenatal testing in Australia: "A more complicated scenario than what I had ever realized".
- Published in:
- Journal of Genetic Counseling, 2023, v. 32, n. 1, p. 213, doi. 10.1002/jgc4.1635
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- Publication type:
- Article
Commentary on 'Life as a Pregnant Genetic Counselor: Take Two'.
- Published in:
- 2012
- By:
- Publication type:
- Opinion
'It's Challenging on a Personal Level'-Exploring the 'Lived Experience' of Australian and Canadian Prenatal Genetic Counselors.
- Published in:
- Journal of Genetic Counseling, 2010, v. 19, n. 6, p. 640, doi. 10.1007/s10897-010-9315-z
- By:
- Publication type:
- Article
Preimplantation Genetic Testing for Monogenic Conditions: Is Cell-Free DNA Testing the Next Step?
- Published in:
- Molecular Diagnosis & Therapy, 2021, v. 25, n. 6, p. 683, doi. 10.1007/s40291-021-00556-0
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- Publication type:
- Article
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Cell-free fetal DNA testing in singleton IVF conceptions.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Cell‐free DNA screening for rare autosomal trisomies and segmental chromosome imbalances.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 11, p. 1349, doi. 10.1002/pd.6233
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- Publication type:
- Article
Ultrasound findings and detection of fetal abnormalities before 11 weeks of gestation.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 13, p. 1675, doi. 10.1002/pd.6055
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- Publication type:
- Article
Outcomes following the detection of fetal edema in early pregnancy prior to non‐invasive prenatal testing.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 2, p. 241, doi. 10.1002/pd.5847
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- Publication type:
- Article
Increasing maternal age is not a significant cause of false‐positive results for monosomy X in non‐invasive prenatal testing.
- Published in:
- Prenatal Diagnosis, 2020, v. 40, n. 11, p. 1466, doi. 10.1002/pd.5790
- By:
- Publication type:
- Article
The importance of ultrasound preceding cell-free DNA screening for fetal chromosomal abnormalities.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Lipiodol flush under ultrasound guidance in Australia.
- Published in:
- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2020, v. 60, n. 6, p. 965, doi. 10.1111/ajo.13244
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- Publication type:
- Article
Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.
- Published in:
- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2016, v. 56, n. 6, p. 605, doi. 10.1111/ajo.12501
- By:
- Publication type:
- Article
Genetic Counselling for PGT.
- Published in:
- 2023
- By:
- Publication type:
- Abstract
Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.975987
- By:
- Publication type:
- Article
Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium.
- Published in:
- Molecular Cytogenetics (17558166), 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13039-024-00677-1
- By:
- Publication type:
- Article
Non-Invasive Prenatal Testing for Sex Chromosome Aneuploidy in Routine Clinical Practice.
- Published in:
- 2018
- By:
- Publication type:
- journal article