Skip to main content
Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis

Fig. 2

CFTR exons 2–3 deletion found in patient 9. a Exons 2–3 deletion in Patient 9 and her mother, which was detected by MLPA. The x-axis shows the genomic positions of the probes, and the y-axis represents the signal ratio compared with control. The red arrow represents the heterozygous deletion. b Quantitative real-time PCR confirmed the CFTR exons 2–3 deletion in the patient, which was inherited from her mother. Experiments were performed in triplicate. c Sanger sequencing revealed a deletion of approximately 13.4 Kb encompassing CFTR exons 2–3. The breakpoints are shown using red lines

Back to article page