Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Indian J Ophthalmol ; 2003 Dec; 51(4): 355-7
Article in English | IMSEAR | ID: sea-70797

ABSTRACT

A case of congenital glaucoma with developmental delay and several dysmorphic features showing 22p+ chromosomal variant is reported.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Aberrations , Chromosomes, Human, Pair 22/genetics , Craniofacial Abnormalities/genetics , Glaucoma/congenital , Humans , Infant , Intraocular Pressure , Karyotyping , Male , Nucleolus Organizer Region/pathology
SELECTION OF CITATIONS
SEARCH DETAIL