| Tài liệu tham khảo |
Loại |
Chi tiết |
| 1. Grinshpun‐Cohen, J., et al., Factors that affect the decision to undergo amniocentesis in women with normal Down syndrome screeningresults: it is all about the age. Health Expectations, 2015. 18(6): p.2306-2317 |
Sách, tạp chí |
| Tiêu đề: |
Factors that affect the decision to undergoamniocentesis in women with normal Down syndrome screening"results: it is all about the age |
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| 2. Savva, G.M., K. Walker, and J.K. Morris, The maternal age‐specific live birth prevalence of trisomies 13 and 18 compared to trisomy 21 (Down syndrome). Prenatal Diagnosis: Published in Affiliation With the International Society for Prenatal Diagnosis, 2010. 30(1): p. 57-64 |
Sách, tạp chí |
| Tiêu đề: |
The maternal age‐specificlive birth prevalence of trisomies 13 and 18 compared to trisomy 21(Down syndrome) |
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| 3. Goldstein, M.L. and S.J. Morewitz, Chronic disorders in children and adolescents. 2011: Springer Science & Business Media |
Sách, tạp chí |
| Tiêu đề: |
Chronic disorders in children andadolescents |
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| 4. Warsof, S.L., S. Larion, and A.Z. Abuhamad, Overview of the impact of noninvasive prenatal testing on diagnostic procedures. Prenatal diagnosis, 2015. 35(10): p. 972-979 |
Sách, tạp chí |
| Tiêu đề: |
Overview of the impactof noninvasive prenatal testing on diagnostic procedures |
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| 5. Allyse, M., et al., Non-invasive prenatal testing: a review ofinternational implementation and challenges. International journal of women's health, 2015. 7: p. 113 |
Sách, tạp chí |
| Tiêu đề: |
Non-invasive prenatal testing: a review of"international implementation and challenges |
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| 6. Đỗ Thị Thanh Thủy, N.T.H.P., Phạm Việt Thanh, Trương Đình Kiệt (2007), “xác lập các giá trị trung vị cho bộ ba xét nghiệm sàng lọc trước sinh bằng kỹ thuât Elisa (gamma kit) trên máy bán tự động”, Tạp chí Y học TP. Hồ Chí Minh, tr 280 – 288 |
Sách, tạp chí |
| Tiêu đề: |
xác lập các giá trị trung vị cho bộ ba xét nghiệm sàng lọctrước sinh bằng kỹ thuât Elisa (gamma kit) trên máy bán tự động |
| Tác giả: |
Đỗ Thị Thanh Thủy, N.T.H.P., Phạm Việt Thanh, Trương Đình Kiệt |
| Năm: |
2007 |
|
| 8. Buckley, S. and B. Sacks, An overview of the development of infants with Down syndrome (0-5 years). 2001: DSE Enterprises |
Sách, tạp chí |
| Tiêu đề: |
An overview of the development of infantswith Down syndrome (0-5 years) |
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| 9. Sherman, S.L., et al., Epidemiology of Down syndrome. Mental retardation and developmental disabilities research reviews, 2007.13(3): p. 221-227 |
Sách, tạp chí |
| Tiêu đề: |
Epidemiology of Down syndrome |
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| 12. Chitayat, D., et al., Double-positive maternal serum screening results for Down syndrome and open neural tube defects: an indicator for fetal structural or chromosomal abnormalities and adverse obstetricoutcomes. American journal of obstetrics and gynecology, 2002 |
Sách, tạp chí |
| Tiêu đề: |
Double-positive maternal serum screening resultsfor Down syndrome and open neural tube defects: an indicator for fetalstructural or chromosomal abnormalities and adverse obstetric"outcomes |
|
| 13. Loane, M., et al., Paper 4: EUROCAT statistical monitoring:identification and investigation of ten year trends of congenital anomalies in Europe. Birth Defects Research Part A: Clinical and Molecular Teratology, 2011. 91(S1): p. S31-S43 |
Sách, tạp chí |
| Tiêu đề: |
Paper 4: EUROCAT statistical monitoring:"identification and investigation of ten year trends of congenitalanomalies in Europe |
|
| 14. Muzzey, D., Understanding the Basics of NGS in the Context of NIPT, in Noninvasive Prenatal Testing (NIPT). 2018, Elsevier. p. 7-24 |
Sách, tạp chí |
| Tiêu đề: |
Understanding the Basics of NGS in the Context of NIPT",in "Noninvasive Prenatal Testing (NIPT) |
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| 15. Taglauer, E., L. Wilkins-Haug, and D. Bianchi, cell-free fetal DNA in the maternal circulation as an indication of placental health and disease. Placenta, 2014. 35: p. S64-S68 |
Sách, tạp chí |
| Tiêu đề: |
cell-free fetal DNA inthe maternal circulation as an indication of placental health anddisease |
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| 16. Stokowski, R., et al., Clinical performance of non‐invasive prenatal testing (NIPT) using targeted cell‐free DNA analysis in maternal plasma with microarrays or next generation sequencing (NGS) is consistent across multiple controlled clinical studies. Prenatal diagnosis, 2015. 35(12): p. 1243-1246 |
Sách, tạp chí |
| Tiêu đề: |
Clinical performance of non‐invasive prenataltesting (NIPT) using targeted cell‐free DNA analysis in maternalplasma with microarrays or next generation sequencing (NGS) isconsistent across multiple controlled clinical studies |
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| 17. Fairbrother, G., et al., Clinical experience of noninvasive prenatal testing with cell‐free DNA for fetal trisomies 21, 18, and 13, in a general screening population. Prenatal diagnosis, 2013. 33(6): p. 580- 583 |
Sách, tạp chí |
| Tiêu đề: |
Clinical experience of noninvasive prenataltesting with cell‐free DNA for fetal trisomies 21, 18, and 13, in ageneral screening population |
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| 18. Bjerregaard, L., et al., The rate of invasive testing for trisomy 21 is reduced after implementation of NIPT. Dan Med J, 2017. 64(4): p.A5359 |
Sách, tạp chí |
| Tiêu đề: |
The rate of invasive testing for trisomy 21 isreduced after implementation of NIPT |
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| 19. Hartwig, T.S., et al., Non-Invasive Prenatal Testing (NIPT) inpregnancies with trisomy 21, 18 and 13 performed in a public setting–factors of importance for correct interpretation of results. European Journal of Obstetrics & Gynecology and Reproductive Biology, 2018 |
Sách, tạp chí |
| Tiêu đề: |
Non-Invasive Prenatal Testing (NIPT) in"pregnancies with trisomy 21, 18 and 13 performed in a public setting–"factors of importance for correct interpretation of results |
|
| 20. Hartwig, T.S., et al., Discordant non‐invasive prenatal testing (NIPT)–a systematic review. Prenatal diagnosis, 2017. 37(6): p. 527-539 |
Sách, tạp chí |
| Tiêu đề: |
Discordant non‐invasive prenatal testing (NIPT)–"a systematic review |
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| 21. Phan, M.-D., et al., Establishing and validating noninvasive prenatal testing procedure for fetal aneuploidies in Vietnam. The Journal of Maternal-Fetal & Neonatal Medicine, 2019. 32(23): p. 4009-4015 |
Sách, tạp chí |
| Tiêu đề: |
Establishing and validating noninvasive prenataltesting procedure for fetal aneuploidies in Vietnam |
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| 22. Langlois, S., et al., Comparison of first‐tier cell‐free DNA screening for common aneuploidies with conventional publically funded screening.Prenatal Diagnosis, 2017. 37(12): p. 1238-1244 |
Sách, tạp chí |
| Tiêu đề: |
Comparison of first‐tier cell‐free DNA screening forcommon aneuploidies with conventional publically funded screening |
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| 7. Đỗ Thị Thanh Thủy, P.V.X., Phùng Nhƣ Toàn, Phạm Việt Thanh, Trương Đình Kiệt, Trần Thị Trung Chiến (2009), “Tầm soát trước sinh hội chứng Down ba tháng giữa thai kỳ bằng hệ thống tự động Immulite 2000 và phần mềm Prisca, Tạp chí Y học TP. Hồ Chí Minh, tr 198 – 203 |
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