Examples of using Subsequent sequencing in English and their translations into Spanish
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respectively and subsequent sequencing.
by PCR amplification and subsequent sequencing of exons 3,
The threading feature will override the subject lines in subsequent sequence steps.
it offers the possibility of sequencing by other genes complete PCR amplification and subsequent sequencing.
using the complete PCR amplification and subsequent sequencing.
by complete PCR amplification of GPR56 gene exons and subsequent sequencing.
in IVAMI perform detection of mutations associated with Bart-Pumphrey syndrome by complete PCR amplification of exons GJB2, and subsequent sequencing.
by complete PCR amplification of the gene exons and subsequent sequencing.
in IVAMI perform detection of mutations associated with Proteus syndrome by complete PCR amplification of AKT1 gene exons and subsequent sequencing.
in IVAMI perform detection of mutations associated with Pelizaeus-Merzbacher disease by the complete PCR amplification of exons PLP1 and subsequent sequencing.
by complete PCR amplification of exons COMP gene, and subsequent sequencing.
IVAMI performed in detecting mutations in the UGT1A1 gene by the complete PCR amplification of the gene exons and subsequent sequencing.
by complete PCR amplification of exons SMARCAD1 gene, and subsequent sequencing.
in IVAMI perform detection of mutations associated with Nijmegen syndrome by complete PCR amplification of exons NBN gene, and subsequent sequencing.
in IVAMI perform detection of mutations associated with Currarino syndrome by complete PCR amplification of exons MNX1 gene, and subsequent sequencing.
by complete PCR amplification of exons FMO3 gene, and subsequent sequencing.
in IVAMI perform detection of mutations associated with Tietz syndrome by complete PCR amplification of exons MITF gene, and subsequent sequencing.
by complete PCR amplification of exons COL2A1 gene, and subsequent sequencing.
associated with Sotos syndrome, by complete PCR amplification of exons NSD1, and subsequent sequencing.
in IVAMI perform detection of mutations associated with Norrie disease by the complete PCR amplification of exons NDP gene and subsequent sequencing.