A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15

Congenital microphthalmia is a common developmental ocular disorder characterized by shortened axial length. Isolated microphthalmia is clinically and genetically heterogeneous and may be inherited in an autosomal dominant, autosomal recessive, or X-linked manner. Here, we studied a five-generation...

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Main Authors: Morlé, L., Bozon, M., Zech, J.-C., Alloisio, N., Raas-Rothschild, A., Philippe, C., Lambert, J.-C., Godet, J., Plauchu, H., Edery, P.
Formáid: Artigo
Teanga:Inglês
Foilsithe: The American Society of Human Genetics 2000
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Report
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287937/
https://ncbi.nlm.nih.gov/pubmed/11035633
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