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Fig. 1 | BMC Pediatrics

Fig. 1

From: Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia

Fig. 1

Direct sequencing analysis revealed the PCR fragment on the δ-globin and β-globin genes. (A), (C1) the arrows indicates the [−CT] deletion at codon 5 in the β-globin gene for the father and the proband respectively; (B1), (C2) the arrows indicates the [−A] deletion at the codon 59 in the δ-globin gene for the mother and the proband respectively; (B2), (C3) the arrows indicates the Hb Knossos substitution at the codon 27 in the β-globin gene for the mother and the proband respectively

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BMC Pediatrics

ISSN: 1471-2431

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