A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor.
- DOI
- 10.17863/cam.112269
- Published
- 2024
- Container
- Not recorded
- Publisher
- Wiley
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.17863/cam.112269,
title = {A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor.},
author = {Mahmood, Shathar and Leiter, Sarah M and Phyu, Poe and Craven, Claudia and Horan, Gail and Gains, Jennifer and Briggs, Mayen and Blanco, Esther and Behjati, Sam and Watkins, James and Tadross, John A and Roberts, Thomas and Trotman, Jamie and Tarpey, Patrick and Armstrong, Ruth and Murray, Matthew J},
year = {2024},
doi = {10.17863/cam.112269},
url = {https://doi.org/10.17863/cam.112269}
}RIS
TY - JOUR TI - A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor. AU - Mahmood, Shathar AU - Leiter, Sarah M AU - Phyu, Poe AU - Craven, Claudia AU - Horan, Gail AU - Gains, Jennifer AU - Briggs, Mayen AU - Blanco, Esther AU - Behjati, Sam AU - Watkins, James AU - Tadross, John A AU - Roberts, Thomas AU - Trotman, Jamie AU - Tarpey, Patrick AU - Armstrong, Ruth AU - Murray, Matthew J PY - 2024 DO - 10.17863/cam.112269 UR - https://doi.org/10.17863/cam.112269 ER -
APA
Shathar, M., M, L. S., Poe, P., Claudia, C., Gail, H., Jennifer, G., Mayen, B., Esther, B., Sam, B., James, W., A, T. J., Thomas, R., Jamie, T., Patrick, T., Ruth, A., & J, M. M. (2024). A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor.. https://doi.org/10.17863/cam.112269
Source records
- datacite · retrieved 2026-11-09T01:23:36.528Z