The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear.
- DOI
- 10.1007/s00234-023-03118-9
- Published
- 2023 Apr
- Container
- Neuroradiology
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s00234-023-03118-9,
title = {The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear.},
author = {Lewis MA and Juliano A and Robson C and Clement E and Nash R and Rajput K and D'Arco F},
year = {2023},
journal = {Neuroradiology},
doi = {10.1007/s00234-023-03118-9},
url = {https://doi.org/10.1007/s00234-023-03118-9}
}RIS
TY - JOUR TI - The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear. AU - Lewis MA AU - Juliano A AU - Robson C AU - Clement E AU - Nash R AU - Rajput K AU - D'Arco F PY - 2023 JO - Neuroradiology DO - 10.1007/s00234-023-03118-9 UR - https://doi.org/10.1007/s00234-023-03118-9 ER -
APA
MA, L., A, J., C, R., E, C., R, N., K, R., & F, D. (2023). The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear.. Neuroradiology. https://doi.org/10.1007/s00234-023-03118-9
Source records
- pubmed · retrieved 2026-09-25T18:54:15.290Z