Re: Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. T. K. Lau, S. W. Cheung, P. S. S. Lo, A. N. Pursley, M. K. Chan, F. Jiang, H. Zhang, W. Wang, L. F. J. Jong, O. K. C. Yuen, H. Y. C. Chan, W. S. K. Chan and K. W. Choy. Ultrasound Obstet Gynecol 2014; 43: 254-264

Ultrasound Obstet Gynecol. 2014 Mar;43(3):245. doi: 10.1002/uog.13314.
No abstract available

Publication types

  • Comment

MeSH terms

  • Chromosome Disorders / diagnosis*
  • Chromosomes, Human, Pair 13
  • Chromosomes, Human, Pair 18
  • DNA / blood*
  • Down Syndrome / diagnosis*
  • Female
  • Humans
  • Mothers*
  • Pregnancy
  • Prenatal Diagnosis*
  • Trisomy / diagnosis*
  • Trisomy 13 Syndrome
  • Trisomy 18 Syndrome

Substances

  • DNA