Abstract
Objective: Chromosomal abnormalities are believed to be a major contributor to the genetic risks of infertility treatment associated with In-vitro Fertilization (IVF). Apart from abnormalities arising de novo, abnormal karyotypes in pregnancies conceived through assisted reproductive technology may be directly derived from predisposing parental aberrations. Our objective was to prospectively assess the frequency of chromosomal aberrations in couples that were candidates entering our IVF/ICSI program.
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