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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
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