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A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis: Can We Put It to Work?

Publication ,  Journal Article
LaBreche, HG; Sebastian, S
Published in: J Mol Diagn
September 2015

This commentary highlights the article by van den Oever et al that describes a new method of prenatal diagnosis of single-mutation disorders.

Duke Scholars

Published In

J Mol Diagn

DOI

EISSN

1943-7811

Publication Date

September 2015

Volume

17

Issue

5

Start / End Page

483 / 486

Location

United States

Related Subject Headings

  • Prenatal Diagnosis
  • Pregnancy
  • Pathology
  • Male
  • Humans
  • Genetic Diseases, Inborn
  • Female
  • Fathers
  • DNA Mutational Analysis
  • 3211 Oncology and carcinogenesis
 

Citation

APA
Chicago
ICMJE
MLA
NLM
LaBreche, H. G., & Sebastian, S. (2015). A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis: Can We Put It to Work? J Mol Diagn, 17(5), 483–486. https://doi.org/10.1016/j.jmoldx.2015.06.002
LaBreche, Heather G., and Siby Sebastian. “A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis: Can We Put It to Work?J Mol Diagn 17, no. 5 (September 2015): 483–86. https://doi.org/10.1016/j.jmoldx.2015.06.002.
LaBreche, Heather G., and Siby Sebastian. “A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis: Can We Put It to Work?J Mol Diagn, vol. 17, no. 5, Sept. 2015, pp. 483–86. Pubmed, doi:10.1016/j.jmoldx.2015.06.002.
Journal cover image

Published In

J Mol Diagn

DOI

EISSN

1943-7811

Publication Date

September 2015

Volume

17

Issue

5

Start / End Page

483 / 486

Location

United States

Related Subject Headings

  • Prenatal Diagnosis
  • Pregnancy
  • Pathology
  • Male
  • Humans
  • Genetic Diseases, Inborn
  • Female
  • Fathers
  • DNA Mutational Analysis
  • 3211 Oncology and carcinogenesis