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Hot Topics of the 19th International Conference on Prenatal Diagnosis and Therapy, 2015, Washington, DC, United States

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Journal of Fetal Medicine

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References

  1. Gross S, Ryan A, Benn P. Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value. Am J Obstet Gynecol. 2015;213(2):254–5.

    Article  PubMed  Google Scholar 

  2. Wapner R, Babiarz J, Levy B, Stosic M, Zimmerman B, Sigurjonsson S, et al. Expanding the scope of non-invasive prenatal testing: detection of fetal microdeletion syndromes. AJOG. 2015;212(3):332e1–9.

    Article  Google Scholar 

  3. Wang J-C, Sahoo T, Schonberg S, Kopita KA, Ross L, Patek K, et al. Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases. Genet Med. 2015;17:234–6.

    Article  CAS  PubMed  Google Scholar 

  4. Benn PA, Chapman AR. Ethical challenges in providing noninvasive prenatal diagnosis. Curr Opin Obstet Gynecol. 2010;22(2):128–34.

    Article  PubMed  Google Scholar 

  5. Yang Y, Muzny D, Xia F, Niu Z, Person R, Ding Y, et al. Molecular findings among patients referred for clinical whole-exome sequencing. JAMA. 2014;312(18):1870–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Drury S, Williams H, Trump N, Boustred C, GOSGene, Lench N, Scott R, Chitty L. Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities. Prenat Diagn. 2015;35(10):1010–7.

    Article  CAS  PubMed  Google Scholar 

  7. ACOG Committee Opinion 640. Cell-free DNA Screening for Fetal Aneuploidy. Obstet Gynecol. 2015.

  8. Gregg AR, Gross SJ, Best RG, Monaghan KG, Bajaj K, Skotko B, et al. ACMG statement on noninvasive prenatal screening for fetal aneuploidy. Genet Med. 2013;15(5):395–8.

    Article  CAS  PubMed  Google Scholar 

  9. Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn. 2015;35(8):725–34.

    Article  PubMed  Google Scholar 

  10. Bianchi D, Chudova D, Sehnert A, Bhatt S, Murray K, Prosen T, et al. Noninvasive prenatal testing and incidental detection of occult maternal malignancies. JAMA. 2015;314(2):162–9.

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Karla Leavitt.

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Leavitt, K. Hot Topics of the 19th International Conference on Prenatal Diagnosis and Therapy, 2015, Washington, DC, United States. J. Fetal Med. 3, 5–8 (2016). https://doi.org/10.1007/s40556-016-0074-2

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  • DOI: https://doi.org/10.1007/s40556-016-0074-2

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