Branchio-oto-renal syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference58 articles.
1. Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1
2. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
3. Slc12a2 is a direct target of two closely related homeobox proteins, Six1 and Six4
4. The eyes absent gene: Genetic control of cell survival and differentiation in the developing Drosophila eye
5. EYA4, a novel vertebrate gene related to Drosophila eyes absent
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