Table 1

Corrections of H19 genomic sequence identified in all patients (n=23) and controls (n=5)

Site Nucleotide position Correct sequence Polymorphism
Exon 11531C→T
Exon 11569T→A
Exon 11737G→A
Intron 22418+CG
Intron 22441+CGG
Intron 22461G→C
Intron 32599+G
Intron 32653−A
Exon 42791G→C
Exon 52894G→A
Exon 52976T→C
Exon 52992T→C
Exon 53238A→G
Exon 53281T→C