Retinal Dystrophy In The Oculo-auricular Syndrome Due to HMX1 Mutation
Author:
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/13816810.2011.562955
Reference6 articles.
1. Cloning, Characterization, and Mapping of the Mouse Homeobox GeneHmx1
2. Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome
3. ISCEV Standard for full-field clinical electroretinography (2008 update)
4. Malformations associées des yeux et des oreilles.
5. The Marshall M. Parks memorial lecture: making sense of early-onset childhood retinal dystrophies--the clinical phenotype of Leber congenital amaurosis
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