{Reference Type}: Case Reports
{Title}: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18.
{Author}: Safavi M;Haghi Ashtiani MT;Badv RS;Azari-Yam A;Vasei M;
{Journal}: Arch Iran Med
{Volume}: 22
{Issue}: 10
{Year}: 10 2019 1
{Factor}: 3.138
{Abstract}: Monosomy 18p syndrome is one of the prototypical examples of autosomal terminal deletions. This deletion can be the consequence of de novo deletions, malsegregation of a balanced parental translocation, cryptic subtelomeric deletions or ring chromosome 18. The present case is a rare cytogenetic variant of monosomy 18 as a consequence of whole-arm translocation between chromosomes 13 and 18 which has been reported only three times previously.