Journal ArticleOPEN ACCESS

Digynic triploidy: utility and challenges of noninvasive prenatal testing

  • Fleischer J
  • Shenoy A
  • Goetzinger K
  • et al.
Clinical Case Reports (2015) 3(6) 406-410
DOI: 10.1002/ccr3.247
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Abstract

Low fraction fetal DNA in noninvasive prenatal testing in the context of fetal growth restriction and multiple congenital anomalies should alert medical professionals to the possibility of digynic triploidy. Single‐nucleotide polymorphism microarray can detect the parental origin of triploidy and explain its mechanism.

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APA

Fleischer, J., Shenoy, A., Goetzinger, K., Cottrell, C. E., Baldridge, D., White, F. V., & Shinawi, M. (2015). Digynic triploidy: utility and challenges of noninvasive prenatal testing. Clinical Case Reports, 3(6), 406–410. https://doi.org/10.1002/ccr3.247

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