Congenital glaucoma associated with 22p+ variant in a dysmorphic child.
Indian J Ophthalmol
; 2003 Dec; 51(4): 355-7
Article
in En
| IMSEAR
| ID: sea-70797
Full text:
1
Index:
IMSEAR
Main subject:
Abnormalities, Multiple
/
Chromosomes, Human, Pair 22
/
Humans
/
Male
/
Glaucoma
/
Chromosome Aberrations
/
Craniofacial Abnormalities
/
Infant
/
Intraocular Pressure
/
Karyotyping
Language:
En
Journal:
Indian J Ophthalmol
Year:
2003
Type:
Article