39 results on '"Stejskal, D."'
Search Results
2. P01.09: The levels of cell‐free fetal DNA in cases of early fetal demise and miscarriage
3. OC06.06: Cell‐free DNA in the detection of chromosomal aneuploidies in early fetal demise and miscarriage
4. OC02.04: Non-commercial cell-free DNA testing in routine clinical aneuploidy screening: a three-year experience
5. OC19.01: Cell-free DNA in the detection of chromosomal aneuploidies in early fetal demise and miscarriage
6. OP22.02: The determination of fetal sex using cell-free DNA testing
7. EP07.10: Talipes equinovarus: prenatal diagnosis and outcome in the centre Gennet 2007-2016, Czech Republic
8. OP08.03; Contingent cell‐free DNA test in routine prenatal aneuploidy screening
9. P09.11: The assessment of the intergrowth biometric charts in unselected Czech population
10. P03.05: Change in the diagnosis and pregnancy outcome of prenatally diagnosed defects of the anterior abdominal wall in Gennet, Prague, Czech Republic
11. OP25.03: Maxillary gap as a first trimester marker of orofacial clefts
12. OP21.09: Risk factors for miscarriage after chorionic villus sampling
13. OC07.10: Is nuchal translucency of 3.0–3.49 mm an indication for NIPT or microarray? Still needs a debate.
14. OP12.02: Modified sequential test for prenatal screening of chromosomal abnormalities: a 5-year study
15. OC05.01: MoM-based approach to non-invasive prenatal testing using exponentially weighted moving average chart and chromosomal fingerprint
16. P11.02: Chorionic villus sampling: an overview of the 11-year period in a single centre and identifying risk factors for miscarriage
17. P10.05: A contribution of SNP array in prenatal diagnosis in 2010–2013
18. P29.12: Hysterosalpingo-foam sonography: a technique to evaluate uterine anomalies and visualise tubal patency
19. OP03.06: The efficacy of real-time nuchal translucency quality review using exponentially weighted moving average chart
20. P01.11: The distribution of nuchal translucency in unaffected pregnancies: a mixture model revisited
21. OC14.02: B-flow technique in the assessment of ductus venosus flow
22. False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism
23. OP28.09: Prenatal detection of Williams-Beuren syndrome using SNP array: report of two cases
24. P06.09: Exponentially weighted moving average chart as a suitable tool for prospective as well as retrospective nuchal translucency quality review
25. P22.04: Rectus sheath hematoma as a rare complication of amniocentesis-report of two cases
26. OP18.01: The influence of fetal sex on parameters of first trimester combined test in normal pregnancies and pregnancies with Down and Edwards syndromes
27. OP19.06: Anomalies of the Muller duct development in women with reproductive disorders
28. OC28.03: Whole-genome SNP array analysis in routine prenatal diagnosis of chromosomal abnormalities - a one-year experience
29. P25.13: Case report of spinal dysraphism with lemon and banana signs in the second trimester and normal intracranial translucency in the first trimester
30. OP08.01: Fetal growth restriction in fetuses with chromosomal anomalies in the first trimester
31. P02.09: New chart for ultrasound dating of pregnancy in the first trimester based on a large sample of Czech population
32. OC009: Evaluation of combined first‐trimester screening ‐ Czech multi‐center study
33. False-negative trisomy 18 non-invasive prenatal test result due to 48, XXX,+18 placental mosaicism.
34. Abstracts of the 26th World Congress on Ultrasound in Obstetrics and Gynecology, Rome, Italy, 24-28 September 2016.
35. Abstracts of the 26th World Congress on Ultrasound in Obstetrics and Gynecology, Rome, Italy, 24-28 September 2016.
36. OP09.03: Crown-rump length measurements during the first trimester screening: Critical evaluation of dating the pregnancy.
37. OP34.04: First-trimester crown-rump length dating chart based on a large sample of exactly dated pregnancies after assisted reproductive technologies.
38. P11.01: Preimplantation diagnosis of monogenic diseases in GENNET.
39. P19.12: Management of abnormal foetus in multiple pregnancies.
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