3p Deletion Syndrome.
| dc.contributor.author | Kaur, Anupam | |
| dc.contributor.author | Khetarpal, S | |
| dc.date.accessioned | 2016-01-06T05:47:35Z | |
| dc.date.available | 2016-01-06T05:47:35Z | |
| dc.date.issued | 2013-08 | |
| dc.description.abstract | 3p 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. | en_US |
| dc.identifier.citation | Kaur Anupam, Khetarpal S. 3p Deletion Syndrome. Indian Pediatrics. 2013 August; 50(8): 795. | en_US |
| dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/169939 | |
| dc.language.iso | en | en_US |
| dc.source.uri | https://www.indianpediatrics.net/aug2013/aug-795-796.htm | en_US |
| dc.subject | 3p deletion | en_US |
| dc.subject | trignocephaly | en_US |
| dc.subject | micrognathia | en_US |
| dc.title | 3p Deletion Syndrome. | en_US |
| dc.type | Article | en_US |