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A whole exome sequencing analysing was carried out on the same six MKD patients followed-up at our children hospital, searching for genetic variants associated with chronic IBD.
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We performed whole-exome sequencing analyses to characterize the genetic landscape of these tumors.
Centralized targeted exome sequencing analyses were performed to detect multiple FGFR mutations and fusions.
This complete OGR1 sequence was confirmed by sequencing analyses.
All constructs were validated by restriction digestions and sequencing analyses.
The mutations were confirmed by DNA sequencing analyses.
Accurate PCR reactions were confirmed by DNA sequencing analyses.
Sequencing analyses were performed using the UNC sequencing facility (University of North Carolina, Chapel Hill).
†Samples subjected to sequencing analyses.
Sequencing analyses confirmed the specificity of these methods.
VE, FL and GA participated in the sequencing analyses.
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