Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
December 5, 2012New England Journal of MedicineOpen Access

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

View Full Paper
Ask AI
Bookmark
Share

Authors

Ronald J. WapnerRonald J. WapnerIntermountain HealthcareAMAlastair J. MartinCardiac ImagingBLBrynn LevyColumbia University Irving Medical Center

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Wapner et al. (2012) studied this question.

synapsesocial.com/papers/69d7f5de7392c8ce61bee4echttps://doi.org/10.1056/nejmoa1203382
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Noninvasive Whole-Genome Sequencing of a Human Fetus2012 · 415 citations
  2. 2Procedure-related miscarriages and down syndrome–affected births: implications for prenatal testing based on women's preferences2000 · 156 citations
  3. 3CONFINED PLACENTAL MOSAICISM FOR TRISOMIES 2, 3, 7, 8, 9, 16, AND 22: THEIR INCIDENCE, LIKELY ORIGINS, AND MECHANISMS FOR CELL LINEAGE COMPARTMENTALIZATION1996 · 193 citations
  4. 4Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants2012 · 648 citations