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Simultaneous Single-Cell Detection of Two Mutations for Cystic Fibrosis

Purpose: A single-cell diagnosis procedure using polymerase chain reaction (PCR) technology was developed to simultaneously detect two cystic fibrosis (CF) mutations (DF-508, W1282X). Methods: Human viable, arrested, and nonviable embryos and immature, and nonfertilized oocytes donated by our patien...

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Detalhes bibliográficos
Main Authors: Drury, K. C., Liu, M. C., Zheng, W., Kipersztok, S., Williams, R. S.
Formato: Artigo
Idioma:Inglês
Publicado em: Kluwer Academic Publishers-Plenum Publishers 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3455267/
https://ncbi.nlm.nih.gov/pubmed/11155327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1023/A:1009450009932
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