Analysing two dinucleotide repeats of FVIII gene in Iranian population

B. Rabbani, A. Rezaeian, H. Khanahmad, R. Bagheri, E. Kamali, Sirous Zeinali

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


Using dinucleotide repeats for carrier detection and prenatal diagnosis of haemophilia A patients, led us to find different alleles and their frequencies in Iranian population. Polymerase chain reaction (PCR) amplification of two short tandem repeat (STR) loci of factor VIII (FVIII) gene was performed, and the PCR products were resolved on 10% native polyacrylamide gel, and samples were analysed with sequenced DNA markers made of PCR cloning of the dinucleotide FVIII gene fragments. Seven different alleles were observed for intron 13 STR, having 18-24 (CA) repeating units and five alleles for intron 22 STR having 24-28 repeating units of (CACT). Bands produced during dinucleotide study were defined in detail so this could improve the genotyping of heterozygotes and homozygotes. Conformational band produced were characterized to specify the dinucleotide pattern. Our results confirm the Hardy-Weinberg proportions of the heterozygosity rate of the 85 analysed individuals. The observed heterozygosity rate for intron 13 and 22 was 52% and 59% respectively. Our data also indicate that our population is closer to caucasians than to any other populations. Finding different dinucleotide repeat alleles and their frequencies has made it possible to identify carriers and provide prenatal diagnosis with more confidence. This allows antenatal diagnosis to be performed in the vast majority of carriers.

Original languageEnglish (US)
Pages (from-to)740-744
Number of pages5
Issue number6
StatePublished - Nov 2007


  • Carrier detection
  • Dinucleotides
  • Factor VIII gene
  • Genetic diagnosis
  • Iranian population
  • Short tandem repeats

ASJC Scopus subject areas

  • Hematology
  • Genetics(clinical)


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