Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.
- DOI
- 10.1097/iop.0b013e3181b59eea
- Published
- 2009 Sep-Oct
- Container
- Ophthalmic plastic and reconstructive surgery
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1097/iop.0b013e3181b59eea,
title = {Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.},
author = {Lane KA and Anninger WV and Katowitz JA},
year = {2009},
journal = {Ophthalmic plastic and reconstructive surgery},
doi = {10.1097/iop.0b013e3181b59eea},
url = {https://doi.org/10.1097/iop.0b013e3181b59eea}
}RIS
TY - JOUR TI - Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations. AU - Lane KA AU - Anninger WV AU - Katowitz JA PY - 2009 JO - Ophthalmic plastic and reconstructive surgery DO - 10.1097/iop.0b013e3181b59eea UR - https://doi.org/10.1097/iop.0b013e3181b59eea ER -
APA
KA, L., WV, A., & JA, K. (2009). Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.. Ophthalmic plastic and reconstructive surgery. https://doi.org/10.1097/iop.0b013e3181b59eea
Source records
- pubmed · retrieved 2026-09-25T04:14:02.051Z