Abramsky, L., & Chapple, J. (2003). Prenatal diagnosis: the human side (2nd ed). Nelson Thornes.
Agathokleous, M., Chaveeva, P., Poon, L. C. Y., & Et al. (2013). Meta-analysis of second-trimester markers for trisomy 21. Ultrasound in Obstetrics & Gynecology, 41(3), 247–261. https://doi.org/10.1002/uog.12364
Alessandra Cacciatore. (2009). Obstetric management in Rh alloimmunizated pregnancy. Journal of Prenatal Medicine, 3(2). https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279102/
American Association for Clinical Chemistry. (n.d.). Clinical chemistry. http://www.clinchem.org/content/by/year
Baillière’s Clinical Obstetrics and Gynaecology. (1987). 1(3). http://www.sciencedirect.com/science/journal/09503552/1/3
Barrett, A. N., McDonnell, T. C. R., Chan, K. C. A., & Chitty, L. S. (2012). Digital PCR Analysis of Maternal Plasma for Noninvasive Detection of Sickle Cell Anemia. Clinical Chemistry, 58(6), 1026–1032. https://doi.org/10.1373/clinchem.2011.178939
Benn, P. A. (2009). Practical and Ethical Considerations of Noninvasive Prenatal Diagnosis. JAMA, 301(20). https://doi.org/10.1001/jama.2009.707
Bianchi, D. W., Platt, L. D., Goldberg, J. D., & Et al. (2012). Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing. Obstetrics & Gynecology, 119(5), 890–901. http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00006250-201205000-00004&LSLINK=80&D=ovft
Celik, E., To, M., Poon, L. C. Y., & Et al. (2008). Cervical length and obstetric history predict spontaneous preterm birth: development and validation of a model to provide individualized risk assessment. Ultrasound in Obstetrics and Gynecology, 31(5), 549–554. https://doi.org/10.1002/uog.5333
Chitty, L. S., van der Schoot, C. E., Hahn, S., & Avent, N. D. (2008). SAFE—TheSpecial Non-invasiveAdvances inFetal and NeonatalEvaluation Network: aims and achievements. Prenatal Diagnosis, 28(2), 83–88. https://doi.org/10.1002/pd.1929
Chudleigh, P., & Thilaganathan, B. (2004). Obstetric ultrasound: how, why and when (3rd ed). Elsevier Churchill Livingstone.
Deans, Z., Clarke, A. J., & Newson, A. J. (2015). For Your Interest? The Ethical Acceptability of Using Non-Invasive Prenatal Testing to Test ‘Purely for Information’. Bioethics, 29(1), 19–25. https://doi.org/10.1111/bioe.12125
Deprest, J., Ghidini, A., Van Mieghem, T., Bianchi, D. W., Faas, B., & Chitty, L. S. (2016). In case you missed it: the editors bring you the most significant advances of 2015. Prenatal Diagnosis, 36(1), 3–9. https://doi.org/10.1002/pd.4758
European Society of Human Genetics. (n.d.). European journal of human genetics: EJHG. [Electronic resource]. http://www.nature.com/ejhg/archive/index.html
Gallo, D. M., Poon, L. C., Akolekar, R., & Et al. (2013). Prediction of Preeclampsia by Uterine Artery Doppler at 20-24 Weeks’ Gestation. Fetal Diagnosis and Therapy, 34(4), 241–247. https://doi.org/10.1159/000356171
Gallo, D., Poon, L. C., Fernandez, M., & Et al. (2014). Prediction of Preeclampsia by Mean Arterial Pressure at 11-13 and 20-24 Weeks’ Gestation. Fetal Diagnosis and Therapy, 36(1), 28–37. https://doi.org/10.1159/000360287
Harrison, M. R., Golbus, M. S., Filly, R. A., & Harrison, M. R. (2001). The unborn patient: the art and science of fetal therapy (3rd ed). Saunders.
Hill, M., Barrett, A. N., White, H., & Chitty, L. S. (2012). Uses of cell free fetal DNA in maternal circulation. Best Practice & Research Clinical Obstetrics & Gynaecology, 26(5), 639–654. https://doi.org/10.1016/j.bpobgyn.2012.03.004
International Fetal Medicine and Surgery Society. (n.d.). Fetal diagnosis and therapy. http://www.karger.com/Journal/Home/224239
International Society for Prenatal Diagnosis. (n.d.). Prenatal diagnosis. Wiley medical publication. http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291097-0223/issues
Journal of Medical Ethics. (1975). http://www.jstor.org/journal/jmedethics
Journal of Prenatal Medicine. (n.d.). https://www.degruyter.com/journal/key/jpme/html?lang=en
Massachusetts Medical Society. (n.d.). The New England journal of medicine. http://www.nejm.org/medical-index
Milunsky, A., & Milunsky, J. M. (Eds.). (2021). Genetic Disorders and the Fetus. John Wiley & Sons Ltd. https://doi.org/10.1002/9781119676980
Nicolaides, K. H. (2011). Turning the Pyramid of Prenatal Care. Fetal Diagnosis and Therapy, 29(3), 183–196. https://doi.org/10.1159/000324320
nipd_june_2016.pdf. (n.d.). http://www.labs.gosh.nhs.uk/media/764057/nipd_june_2016.pdf
Pandya, P. P., Wapner, R., Oepkes, D., & Sebire, N. J. (Eds.). (2020). Fetal medicine: basic science and clinical practice (Third edition). Elsevier. https://www.sciencedirect.com/science/book/9780702069567
PloS one. (n.d.). https://journals.plos.org/plosone/
Ravitsky, V. (2009). Non-invasive prenatal diagnosis: an ethical imperative. Nature Reviews Genetics, 10(10), 733–733. https://doi.org/10.1038/nrg2631-c1
Sadler, T. W. (2015). Langman’s medical embryology (Thirteenth edition, International edition). Wolters Kluwer.
Simpson, J. L., & Elias, S. (1993). Essentials of prenatal diagnosis. Churchill Livingstone.
Smith, N. C., Smith, A. P. M., & Smith, N. C. (2006). Obstetric and gynaecological ultrasound made easy (2nd ed). Elsevier Churchill Livingstone.
Sparks, A. B., Wang, E. T., Struble, C. A., & Et al. (2012). Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy. Prenatal Diagnosis, 32(1), 3–9. https://doi.org/10.1002/pd.2922
Syngelaki, A., Chelemen, T., Dagklis, T., & Et al. (2011). Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks. Prenatal Diagnosis, 31(1), 90–102. https://doi.org/10.1002/pd.2642
Syngelaki, A., Pergament, E., Homfray, T., & Et al. (2014). Replacing the Combined Test by Cell-Free DNA Testing in Screening for Trisomies 21, 18 and 13: Impact on the Diagnosis of Other Chromosomal Abnormalities. Fetal Diagnosis and Therapy, 35(3), 174–184. https://doi.org/10.1159/000358388
Wald, N. J., & Bestwick, J. P. (2015). Performance of antenatal reflex DNA screening for Down’s syndrome. Journal of Medical Screening, 22(4), 168–174. https://doi.org/10.1177/0969141315581005
Wright, C. F., & Burton, H. (2008). The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis. Human Reproduction Update, 15(1), 139–151. https://doi.org/10.1093/humupd/dmn047
