35 results on '"Benn, Peter"'
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2. P651: Bleeding complications in pregnant carriers of factor IX and factor XI ascertained through carrier screening
3. Correspondence on “Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions” by Hoskovec et al
4. Cell-free DNA screening for fetal aneuploidy as a clinical service
5. CHROMOSOME MOSAICISM IN PRODUCTS OF CONCEPTION SAMPLES
6. 1152 Positive Carrier Screening for Alport Syndrome: A Need for Greater Awareness
7. 250 Preimplantation genetic testing (PGT) for non-homologous Robertsonian translocation carriers: a twelve-year laboratory experience
8. 143 Accuracy of fetal fraction measurements in SNP-based non-invasive prenatal testing (NIPT)
9. The Role of Second-Trimester Serum Screening in the Post–First-Trimester Screening Era
10. Posttest risk calculation following positive noninvasive prenatal screening using cell-free DNA in maternal plasma
11. On the genesis and prognosis of variant translocations in chronic myeloid leukemia
12. Down Syndrome Screening in the First and/or Second Trimester: Model Predicted Performance Using Meta-Analysis Parameters
13. Incorporation of inhibin-A in second-trimester screening for Down syndrome
14. Combined second-trimester biochemical and ultrasound screening for Down syndrome
15. Efficacy of screening for fetal down syndrome in the United States from 1974 to 1997
16. Cost-effectiveness of estimating gestational age by ultrasonography in Down syndrome screening
17. Maternal serum screening for fetal trisomy 18: a comparison of fixed cutoff and patient-specific risk protocols
18. Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities
19. Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value
20. Reply
21. 722: Follow-up frequency of testing in patients at very low risk for Trisomy 21 on first trimester screening
22. 721: Comparison of two protocols for ultrasound markers in Down syndrome screening by the genetic sonogram
23. 701: Follow-up testing of first trimester patients who screen positive for trisomy 21
24. Prenatally Diagnosed Sacrococcygeal Teratoma: A Unique Expression of Trisomy 1q
25. What is the real risk for trisomy 18?
26. Nuchal fold thickness as a marker for congenital cardiac anomalies
27. How to combine first- and second-trimester down syndrome screening tests
28. Down syndrome live births in the U. S. from 1989 to 2001
29. Review of the cytogenetic changes in acute megakaryoblastic leukemia: One disease or several?
30. A new translocation involving chromosomes 8 and 9 in a Philadelphia-negative chronic myelogenous leukemia
31. Dual Genotype in Cutaneous T Cell Lymphoma: Immunoglobulin Gene Rearrangement in Clonal T Cell Malignancy
32. BCR-ABL BREAKPOINT AND PROGNOSIS IN CHRONIC MYELOID LEUKEMIA: RESPONSE
33. RESPONSE
34. bcr BREAKPOINT AND PROGNOSIS OF CHRONIC PHASE CHRONIC MYELOID LEUKEMIA
35. Reply
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