Whole-genome copy number variation analysis in anophthalmia and microphthalmia

Anophthalmia and microphthalmia (A/M) represent severe developmental ocular malformations. Currently, mutations in known genes explain less than 40% of A/M cases. We performed whole genome copy number variation analysis in sixty patients affected with isolated or syndromic A/M. Pathogenic deletions...

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Main Authors: Schilter, Kala F., Reis, Linda M., Schneider, Adele, Bardakjian, Tanya M., Abdul-Rahman, Omar, Kozel, Beth A., Zimmerman, Holly H., Broeckel, Ulrich, Semina, Elena V.
Formato: Artigo
Idioma:Inglês
Publicado: 2013
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3985344/
https://ncbi.nlm.nih.gov/pubmed/23701296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12202
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