A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.

Congenital microphthalmia (CMIC) (OMIM 309700) may occur in isolation or in association with a variety of systemic malformations. Isolated CMIC may be inherited as an autosomal dominant, an autosomal recessive, or an X-linked trait. On the basis of a whole-genome linkage analysis, we have mapped the...

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Autores principales: Bessant, D A, Khaliq, S, Hameed, A, Anwar, K, Mehdi, S Q, Payne, A M, Bhattacharya, S S
Formato: Artigo
Lenguaje:Inglês
Publicado: 1998
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377100/
https://ncbi.nlm.nih.gov/pubmed/9545413
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