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Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort

Academic Article
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Overview

authors

  • Pergament, E.
  • Cuckle, H.
  • Zimmermann, B.
  • Banjevic, M.
  • Sigurjonsson, S.
  • Ryan, A.
  • Hall, M. P.
  • Dodd, M.
  • Lacroute, P.
  • Stosic, M.
  • Chopra, N.
  • Hunkapiller, N.
  • Prosen, D. E.
  • McAdoo, S.
  • Demko, Zachary
  • Siddiqui, A.
  • Hill, M.
  • Rabinowitz, M.

publication date

  • August 2014

journal

  • Obstetrics and Gynecology  Journal

subject areas

  • Adolescent
  • Adult
  • Algorithms
  • Aneuploidy
  • Cell-Free System
  • Chromosome Disorders
  • Chromosomes, Human, Pair 13
  • Chromosomes, Human, Pair 18
  • DNA
  • Down Syndrome
  • Female
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Pregnancy
  • Prenatal Diagnosis
  • Risk Factors
  • Sensitivity and Specificity
  • Trisomy
  • Turner Syndrome
  • Young Adult
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Identity

PubMed Central ID

  • PMC4144440

International Standard Serial Number (ISSN)

  • 0029-7844

Digital Object Identifier (DOI)

  • 10.1097/aog.0000000000000363

PubMed ID

  • 25004354
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Additional Document Info

start page

  • 210

end page

  • 218

volume

  • 124

issue

  • 2

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