Kaur, AnupamKhetarpal, S2016-01-062016-01-062013-08Kaur Anupam, Khetarpal S. 3p Deletion Syndrome. Indian Pediatrics. 2013 August; 50(8): 795.http://imsear.searo.who.int/handle/123456789/1699393p deletion is a rare cytogenetic finding. Here we describe a 3 months old male with congenital malformations. His karyotype revealed 3p deletion 46,XY,del(3)(p25-pter). The child had flexion deformity of wrist and elbow which has never been reported before.en3p deletiontrignocephalymicrognathiaArticle