Bibliography for IFWHG006: Prenatal Diagnosis and Screening BETA

Abramsky, L. and Chapple, J. (2003) Prenatal diagnosis: the human side. 2nd ed. Cheltenham, U.K.: Nelson Thornes.

Agathokleous, M. et al. (2013) ‘Meta-analysis of second-trimester markers for trisomy 21’, Ultrasound in Obstetrics & Gynecology, 41(3), pp. 247–261. Available at: https://doi.org/10.1002/uog.12364.

Alessandra Cacciatore (2009) ‘Obstetric management in Rh alloimmunizated pregnancy’, Journal of Prenatal Medicine, 3(2). Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279102/.

American Association for Clinical Chemistry (no date) ‘Clinical chemistry’. Available at: http://www.clinchem.org/content/by/year.

‘Baillière’s Clinical Obstetrics and Gynaecology’ (1987), 1(3). Available at: http://www.sciencedirect.com/science/journal/09503552/1/3.

Barrett, A.N. et al. (2012) ‘Digital PCR Analysis of Maternal Plasma for Noninvasive Detection of Sickle Cell Anemia’, Clinical Chemistry, 58(6), pp. 1026–1032. Available at: https://doi.org/10.1373/clinchem.2011.178939.

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

Bianchi, D.W. et al. (2012) ‘Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing’, Obstetrics & Gynecology, 119(5), pp. 890–901. Available at: http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00006250-201205000-00004&LSLINK=80&D=ovft.

Celik, E. 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), pp. 549–554. Available at: https://doi.org/10.1002/uog.5333.

Chitty, L.S. et al. (2008) ‘SAFE—TheSpecial Non-invasiveAdvances inFetal and NeonatalEvaluation Network: aims and achievements’, Prenatal Diagnosis, 28(2), pp. 83–88. Available at: https://doi.org/10.1002/pd.1929.

Chudleigh, P. and Thilaganathan, B. (2004) Obstetric ultrasound: how, why and when. 3rd ed. Edinburgh: Elsevier Churchill Livingstone.

Deans, Z., Clarke, A.J. and Newson, A.J. (2015) ‘For Your Interest? The Ethical Acceptability of Using Non-Invasive Prenatal Testing to Test “Purely for Information”’, Bioethics, 29(1), pp. 19–25. Available at: https://doi.org/10.1111/bioe.12125.

Deprest, J. et al. (2016) ‘In case you missed it: the  editors bring you the most significant advances of 2015’, Prenatal Diagnosis, 36(1), pp. 3–9. Available at: https://doi.org/10.1002/pd.4758.

European Society of Human Genetics (no date) ‘European journal of human genetics: EJHG.’ Available at: http://www.nature.com/ejhg/archive/index.html.

Gallo, D. et al. (2014) ‘Prediction of Preeclampsia by Mean Arterial Pressure at 11-13 and 20-24 Weeks’ Gestation’, Fetal Diagnosis and Therapy, 36(1), pp. 28–37. Available at: https://doi.org/10.1159/000360287.

Gallo, D.M. et al. (2013) ‘Prediction of Preeclampsia by Uterine Artery Doppler at 20-24 Weeks’ Gestation’, Fetal Diagnosis and Therapy, 34(4), pp. 241–247. Available at: https://doi.org/10.1159/000356171.

Harrison, M.R. et al. (2001) The unborn patient: the art and science of fetal therapy. 3rd ed. Philadelphia: Saunders.

Hill, M. et al. (2012) ‘Uses of cell free fetal DNA in maternal circulation’, Best Practice & Research Clinical Obstetrics & Gynaecology, 26(5), pp. 639–654. Available at: https://doi.org/10.1016/j.bpobgyn.2012.03.004.

International Fetal Medicine and Surgery Society (no date) ‘Fetal diagnosis and therapy’. Available at: http://www.karger.com/Journal/Home/224239.

International Society for Prenatal Diagnosis (no date) ‘Prenatal diagnosis’, Wiley medical publication. Available at: http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291097-0223/issues.

‘Journal of Medical Ethics’ (1975). Available at: http://www.jstor.org/journal/jmedethics.

‘Journal of Prenatal Medicine’ (no date). Available at: https://www.degruyter.com/journal/key/jpme/html?lang=en.

Massachusetts Medical Society (no date) ‘The New England journal of medicine’. Available at: http://www.nejm.org/medical-index.

Milunsky, A. and Milunsky, J.M. (eds) (2021) Genetic Disorders and the Fetus. Oxford, UK: John Wiley & Sons Ltd. Available at: https://doi.org/10.1002/9781119676980.

Nicolaides, K.H. (2011) ‘Turning the Pyramid of Prenatal Care’, Fetal Diagnosis and Therapy, 29(3), pp. 183–196. Available at: https://doi.org/10.1159/000324320.

‘nipd_june_2016.pdf’ (no date). Available at: http://www.labs.gosh.nhs.uk/media/764057/nipd_june_2016.pdf.

Pandya, P.P. et al. (eds) (2020) Fetal medicine: basic science and clinical practice. Third edition. [London?]: Elsevier. Available at: https://www.sciencedirect.com/science/book/9780702069567.

‘PloS one’ (no date). Available at: https://journals.plos.org/plosone/.

Ravitsky, V. (2009) ‘Non-invasive prenatal diagnosis: an ethical imperative’, Nature Reviews Genetics, 10(10), pp. 733–733. Available at: https://doi.org/10.1038/nrg2631-c1.

Sadler, T.W. (2015) Langman’s medical embryology. Thirteenth edition, International edition. Philadelphia: Wolters Kluwer.

Simpson, J.L. and Elias, S. (1993) Essentials of prenatal diagnosis. New York: Churchill Livingstone.

Smith, N.C., Smith, A.P.M. and Smith, N.C. (2006) Obstetric and gynaecological ultrasound made easy. 2nd ed. Edinburgh: Elsevier Churchill Livingstone.

Sparks, A.B. et al. (2012) ‘Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy’, Prenatal Diagnosis, 32(1), pp. 3–9. Available at: https://doi.org/10.1002/pd.2922.

Syngelaki, A. et al. (2011) ‘Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks’, Prenatal Diagnosis, 31(1), pp. 90–102. Available at: https://doi.org/10.1002/pd.2642.

Syngelaki, A. 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), pp. 174–184. Available at: https://doi.org/10.1159/000358388.

Wald, N.J. and Bestwick, J.P. (2015) ‘Performance of antenatal reflex DNA screening for Down’s syndrome’, Journal of Medical Screening, 22(4), pp. 168–174. Available at: https://doi.org/10.1177/0969141315581005.

Wright, C.F. and Burton, H. (2008) ‘The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis’, Human Reproduction Update, 15(1), pp. 139–151. Available at: https://doi.org/10.1093/humupd/dmn047.