3p Deletion Syndrome.
Indian Pediatr
;
2013 August; 50(8): 795
Artículo
en Inglés
| 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.
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Índice:
IMSEAR (Asia Sudoriental)
Idioma:
Inglés
Revista:
Indian Pediatr
Año:
2013
Tipo del documento:
Artículo
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