Response to “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”

Shranjeno v:
Bibliografske podrobnosti
izdano v:Prenat Diagn
Main Authors: Muzzey, Dale, Haverty, Carrie, Evans, Eric A., Goldberg, James D.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2017
Teme:
Correspondence
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5811916/
https://ncbi.nlm.nih.gov/pubmed/28675624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.5071
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