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The genetic architecture of aniridia and Gillespie syndrome
Absence of part or all of the iris, aniridia, is a feature of several genetically distinct conditions. This review focuses on iris development and then the clinical features and molecular genetics of these iris malformations. Classical aniridia, a panocular eye malformation including foveal hypoplas...
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| Yayımlandı: | Hum Genet |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Springer Berlin Heidelberg
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6710220/ https://ncbi.nlm.nih.gov/pubmed/30242502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-018-1934-8 |
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