Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

BACKGROUND—Congenital microphthalmia (OMIM: 309700) may occur in isolation or in association with a variety of systemic malformations. Isolated microphthalmia may be inherited as an autosomal dominant, an autosomal recessive, or an X linked trait.
METHODS—Based on a whole genome linkage analysis, in...

Full description

Saved in:
Bibliographic Details
Main Authors: Bessant, D., Anwar, K., Khaliq, S., Hameed, A., Ismail, M, Payne, A., Mehdi, S, Bhattacharya, S.
Format: Artigo
Language:Inglês
Published: 1999
Subjects:
Original articles - Clinical science
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1723146/
https://ncbi.nlm.nih.gov/pubmed/10413693
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items