33 results on '"Kucińska‐Chahwan, Anna"'
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2. Using cluster analysis to determine different sonographic phenotypes of fetal complex ventral wall malformations
3. Maternal thyroid function and free beta human chorionic gonadotrophin level in triploid pregnancies of paternal origin
4. Distribution of diandric and digynic triploidy depending on gestational age
5. Usefulness of methylation-specific multiplex ligation-dependent probe amplification for identification of parental origin of triploidy
6. A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC)
7. In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland
8. Prenatal diagnosis of Emanuel syndrome – case series and review of the literature
9. Complex malformations involving the fetal body wall – definition and classification issues
10. Prenatal diagnosis of acrania/exencephaly/anencephaly sequence (AEAS): additional structural and genetic anomalies
11. Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience
12. Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies
13. Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities
14. Clinical significance of the prenatal double bubble sign – single institution experience
15. Triploid pregnancy–Clinical implications
16. A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC).
17. Twin pregnancies discordant for digynic triploidy – A case series
18. A Placental Trisomy 2 Detected by NIPT Evolved in a Fetal Small Supernumerary Marker Chromosome (sSMC).
19. Prenatal diagnosis and clinical significance of cephalocele—A single institution experience and literature review
20. The role of ultrasound and genetic counsel in prenatal diagnosis of split hand/foot malformation with long bone deficiency
21. The location of the fetal ears: A hint for prenatal diagnosis of agnathia‐otocephaly complex
22. Targeted prenatal diagnosis of Pallister-Killian syndrome
23. Blue Rubber Bleb Nevus Syndrome Diagnosed Prenatally as an Epignathus
24. Non-invasive prenatal diagnosis of the most common aneuploidies with cell-free fetal DNA in maternal serum – preliminary results
25. Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3–7p15.3, including TWIST1 gene – a case report
26. Maternal blood intrauterine transfusions in the therapy of red-cell alloimmunization performed in three difficult cases
27. [Aberrant right subclavian artery (ARSA)--a new sonographic marker for chromosomal aberrations in the second trimester--preliminary observations].
28. [Maternal blood intrauterine transfusions in the therapy of red-cell alloimmunization performed in three difficult cases].
29. Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3-7p15.3, including TWIST1 gene--a case report.
30. [Non-invasive prenatal diagnosis of the most common aneuploidies with cell-free fetal DNA in maternal serum--preliminary results].
31. [Analysis of ultrasonic scans and karyotype of fetuses with holoprosencephaly diagnosed in the Department of Obstetrics & Gynecology of the Postgraduate Center of Medical Education between 1997 & 2005].
32. [Anterior abdominal wall defects--retrospective analysis of fetuses diagnosed in the Department of Obstetrics & Gynecology of the Postgraduate Center of Medical Education between 1997 & 2002].
33. [Ventriculomegaly without dysraphic malformations--retrospective analysis fetuses diagnosed in the Department of Gynecology & Obstetrics of the Postgraduate Center of Medical Education in Warsaw, between 1997-2002].
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