21 results on '"Kucińska‐Chahwan, Anna"'
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2. Distribution of diandric and digynic triploidy depending on gestational age
3. Usefulness of methylation-specific multiplex ligation-dependent probe amplification for identification of parental origin of triploidy
4. A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC)
5. 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
6. Using cluster analysis to determine different sonographic phenotypes of fetal complex ventral wall malformations
7. Maternal thyroid function and free beta human chorionic gonadotrophin level in triploid pregnancies of paternal origin
8. Complex malformations involving the fetal body wall – definition and classification issues
9. Prenatal diagnosis of Emanuel syndrome – case series and review of the literature.
10. Clinical significance of the prenatal double bubble sign – single institution experience
11. Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience.
12. Prenatal diagnosis and clinical significance of cephalocele-A single institution experience and literature review.
13. Triploid pregnancy–Clinical implications.
14. The location of the fetal ears: A hint for prenatal diagnosis of agnathia-otocephaly complex.
15. Targeted prenatal diagnosis of Pallister-Killian syndrome.
16. Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.
17. Blue Rubber Bleb Nevus Syndrome Diagnosed Prenatally as an Epignathus.
18. Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
19. Twin pregnancies discordant for digynic triploidy - A case series.
20. The role of ultrasound and genetic counsel in prenatal diagnosis of split hand/foot malformation with long bone deficiency.
21. 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.
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