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21 results on '"Egbert, Melissa"'

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1. The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia: Artificial Intelligence Model

2. Performance of prenatal cfDNA screening for sex chromosomes

3. Validation of a Single-Nucleotide Polymorphism-Based Non-Invasive Prenatal Test in Twin Gestations: Determination of Zygosity, Individual Fetal Sex, and Fetal Aneuploidy.

4. Obstetrical, Perinatal, and Genetic Outcomes Associated With Nonreportable Prenatal Cell-Free DNA Screening Results

6. 866 Zygosity-based Twin Pregnancy Outcomes: Insights from SNP-Based cfDNA Screening

7. 1117 SNP-based Prenatal Cell-free DNA Screening in Twin Pregnancies: A New Standard of Care?

8. 989 Maternal and ultrasound characteristics associated with persistence of cell-free DNA from a vanishing twin pregnancy

9. Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study

10. Cell-free DNA screening for trisomies 21, 18, and 13 in pregnancies at low and high risk for aneuploidy with genetic confirmation

11. Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome

12. Obstetrical, perinatal and genetic outcomes associated with non-reportable prenatal cell free DNA screening results

14. CLINICAL SAFETY OF EGD WITH CONSCIOUS SEDATION IN MODERATE VS. SEVERELY OBESE PATIENTS: ANALYSIS FROM NATIONAL MULITCENTER RESEARCH NETWORK

15. cfDNA prenatal screening for Cri-Du-Chat, Prader-Willi/Angelman and 1p36del syndromes in 10,971 pregnancies with genetic confirmation

16. Performance of ultrasound, maternal serum screening and cell-free DNA for the detection of 22q11.2 deletion syndrome

17. 67 Multicenter prospective study of SNP-based cfDNA for 22q11.2 deletion in 18,289 pregnancies with genetic confirmation

18. 5 Perinatal and genetic outcomes associated with no call cfDNA results in 18,496 pregnancies

20. Cover Image.

21. OP477 - Performance of ultrasound, maternal serum screening and cell-free DNA for the detection of 22q11.2 deletion syndrome.

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