Phenotypical characterization of 13q deletion syndrome: Report of two cases
We present two cases with 13q syndrome with two different deleted region and different severity on clinical features: One case with interstitial deletion belongs to the Group 1 with mild mental retardation and minor malformations and the other case with terminal deletion belongs to Group 3 with moderate to severe mental retardation and major malformations.
Source: Indian Journal of Human Genetics - Category: Genetics & Stem Cells Authors: Eiman BagherizadehYousef ShafaghatiFatemeh HadipourFarkhondeh Behjati Source Type: research