Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children

Figures & data

Figure 1 Direct DNA sequencing of the F7 gene in our study revealed homozygous C.681+1G>T (IVS6+1G>T) mutation in Patients 1 and 4 (A), compound heterozygous c.291+2T>C (IVS2+2T>C) (B), and c.1126A>T (p.K376X) (C) mutations in Patient 2, and homozygous c.1126A>T (p.K376X) (D) mutation in Patient 3.