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Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients
Most 22q11.2 deletion syndrome (22q11DS) patients have middle and outer ear anomalies, whereas some have inner ear malformations. Tbx1, a gene hemizygously deleted in 22q11DS patients and required for ear development, is expressed in multiple tissues during embryogenesis. To determine the role of Tb...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2563157/ https://ncbi.nlm.nih.gov/pubmed/16600992 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddl084 |
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