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...

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Main Authors: Bessant, D., Anwar, K., Khaliq, S., Hameed, A., Ismail, M, Payne, A., Mehdi, S, Bhattacharya, S.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 1999
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Original articles - Clinical science
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1723146/
https://ncbi.nlm.nih.gov/pubmed/10413693
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