Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations
- DOI
- 10.1186/s12881-020-0986-5
- Published
- 2020-03-12
- Container
- BMC Medical Genetics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s12881-020-0986-5,
title = {Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations},
author = {Jeevana Praharsha Athota and Meenakshi Bhat and Sheela Nampoothiri and Kalpana Gowrishankar and Sanjeeva Ghanti Narayanachar and Vinuth Puttamallesh and Mohammed Oomer Farooque and Swathi Shetty},
year = {2020},
journal = {BMC Medical Genetics},
doi = {10.1186/s12881-020-0986-5},
url = {https://doi.org/10.1186/s12881-020-0986-5}
}RIS
TY - JOUR TI - Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations AU - Jeevana Praharsha Athota AU - Meenakshi Bhat AU - Sheela Nampoothiri AU - Kalpana Gowrishankar AU - Sanjeeva Ghanti Narayanachar AU - Vinuth Puttamallesh AU - Mohammed Oomer Farooque AU - Swathi Shetty PY - 2020 JO - BMC Medical Genetics DO - 10.1186/s12881-020-0986-5 UR - https://doi.org/10.1186/s12881-020-0986-5 ER -
APA
Athota, J. P., Bhat, M., Nampoothiri, S., Gowrishankar, K., Narayanachar, S. G., Puttamallesh, V., Farooque, M. O., & Shetty, S. (2020). Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations. BMC Medical Genetics. https://doi.org/10.1186/s12881-020-0986-5
Source records
- crossref · retrieved 2026-09-26T20:52:22.426Z