Bibliography for IFWHG006: Prenatal Diagnosis and Screening BETA

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Benn, Peter A. 2009. ‘Practical and Ethical Considerations of Noninvasive Prenatal Diagnosis’. JAMA 301 (20). https://doi.org/10.1001/jama.2009.707.

Bianchi, Diana W., Lawrence D. Platt, James D. Goldberg, and 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., M. To, L. C. Y. Poon, and 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): 549–54. https://doi.org/10.1002/uog.5333.

Chitty, Lyn S., C. Ellen van der Schoot, Sinuhe Hahn, and Neil D. Avent. 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, Patricia, and Basky Thilaganathan. 2004. Obstetric Ultrasound: How, Why and When. 3rd ed. Edinburgh: Elsevier Churchill Livingstone.

Deans, Zuzana, Angus J. Clarke, and Ainsley J. Newson. 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, Jan, Alessandro Ghidini, Tim Van Mieghem, Diana W. Bianchi, Brigitte Faas, and Lyn S. Chitty. 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.

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Gallo, Dahiana Marcela, Leona C. Poon, Ranjit Akolekar, and Et al. 2013. ‘Prediction of Preeclampsia by Uterine Artery Doppler at 20-24 Weeks’ Gestation’. Fetal Diagnosis and Therapy 34 (4): 241–47. https://doi.org/10.1159/000356171.

Gallo, Dahiana, Leona C. Poon, Mariana Fernandez, and 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, Michael R., Mitchell S. Golbus, Roy A. Filly, and Michael R. Harrison. 2001. The Unborn Patient: The Art and Science of Fetal Therapy. 3rd ed. Philadelphia: Saunders.

Hill, Melissa, Angela N. Barrett, Helen White, and Lyn S. Chitty. 2012. ‘Uses of Cell Free Fetal DNA in Maternal Circulation’. Best Practice & Research Clinical Obstetrics & Gynaecology 26 (5): 639–54. https://doi.org/10.1016/j.bpobgyn.2012.03.004.

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Milunsky, Aubrey, and Jeff M. Milunsky, eds. 2021. Genetic Disorders and the Fetus. Oxford, UK: John Wiley & Sons Ltd. https://doi.org/10.1002/9781119676980.

Nicolaides, Kypros H. 2011. ‘Turning the Pyramid of Prenatal Care’. Fetal Diagnosis and Therapy 29 (3): 183–96. https://doi.org/10.1159/000324320.

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Simpson, Joe Leigh, and Sherman Elias. 1993. Essentials of Prenatal Diagnosis. New York: Churchill Livingstone.

Smith, N. C., A. Pat M. Smith, and N. C. Smith. 2006. Obstetric and Gynaecological Ultrasound Made Easy. 2nd ed. Edinburgh: Elsevier Churchill Livingstone.

Sparks, Andrew B., Eric T. Wang, Craig A. Struble, and 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, Argyro, Teodora Chelemen, Themistoklis Dagklis, and 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, Argyro, Eugene Pergament, Tessa Homfray, and 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): 174–84. https://doi.org/10.1159/000358388.

Wald, Nicholas J, and Jonathan P Bestwick. 2015. ‘Performance of Antenatal Reflex DNA Screening for Down’s Syndrome’. Journal of Medical Screening 22 (4): 168–74. https://doi.org/10.1177/0969141315581005.

Wright, C. F., and H. Burton. 2008. ‘The Use of Cell-Free Fetal Nucleic Acids in Maternal Blood for Non-Invasive Prenatal Diagnosis’. Human Reproduction Update 15 (1): 139–51. https://doi.org/10.1093/humupd/dmn047.