3p Deletion Syndrome.
Indian Pediatr
;
2013 August; 50(8): 795
Article
in English
| IMSEAR
| ID: sea-169939
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian Pediatr
Year:
2013
Type:
Article
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