Works matching AU Srebniak, M.I.
Results: 8
OC07.10: Is nuchal translucency of 3.0–3.49 mm an indication for NIPT or microarray? Still needs a debate.
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- Ultrasound in Obstetrics & Gynecology, 2022, v. 60, p. 23, doi. 10.1002/uog.25047
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- Article
P16.04: Prevalence of submicroscopic chromosome aberrations in pregnancies without increased risk for structural chromosome aberrations: a systematic review of the literature.
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- Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 205, doi. 10.1002/uog.18158
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- Article
P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high-risk pregnancies without ultrasound anomalies.
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- Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 206, doi. 10.1002/uog.18159
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- Article
EP06.03: Be aware of a diagnostic delay: Rotterdam's experience with NIPT in 1071 high-risk pregnancies.
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- Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 284, doi. 10.1002/uog.18407
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- Article
P13.04: Does genomic microarray add prognostic information in case of the second trimester small-for-gestational age, but structurally normal fetus?
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 254, doi. 10.1002/uog.14234
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- Article
OP35.10: What do pregnant couples want? The preferences of pregnant couples at increased risk for Down's syndrome who are offered a choice in prenatal diagnosis between the clinical outcomes of 5 Mb and 0,5 Mb whole genome SNP array analysis.
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 148, doi. 10.1002/uog.13984
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- Article
Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
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- Clinical Genetics, 2015, v. 88, n. 1, p. 25, doi. 10.1111/cge.12479
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- Article
Another Rare Case of a Child with de novo Terminal 9p Deletion and Co-Existing Interstitial 9p Duplication: Clinical Findings and Molecular Cytogenetic Study by Array-CGH.
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- Cytogenetic & Genome Research, 2012, v. 139, n. 1, p. 9, doi. 10.1159/000342165
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- Article