A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype.

Aliferis K, Stoetzel C, Pelletier V, Hellé S, Angioï-Duprez K, Vigneron J, Leheup B, Marion V, Dollfus H

DOI: 10.3109/13816810.2011.592176
Published: 2011 Nov
Container: Ophthalmic genetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3109/13816810.2011.592176,
  title = {A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype.},
  author = {Aliferis K and Stoetzel C and Pelletier V and Hellé S and Angioï-Duprez K and Vigneron J and Leheup B and Marion V and Dollfus H},
  year = {2011},
  journal = {Ophthalmic genetics},
  doi = {10.3109/13816810.2011.592176},
  url = {https://doi.org/10.3109/13816810.2011.592176}
}

RIS

TY  - JOUR
TI  - A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype.
AU  - Aliferis K
AU  - Stoetzel C
AU  - Pelletier V
AU  - Hellé S
AU  - Angioï-Duprez K
AU  - Vigneron J
AU  - Leheup B
AU  - Marion V
AU  - Dollfus H
PY  - 2011
JO  - Ophthalmic genetics
DO  - 10.3109/13816810.2011.592176
UR  - https://doi.org/10.3109/13816810.2011.592176
ER  -

APA

K, A., C, S., V, P., S, H., K, A., J, V., B, L., V, M., & H, D. (2011). A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype.. Ophthalmic genetics. https://doi.org/10.3109/13816810.2011.592176

Source records

pubmed · retrieved 2026-11-10T13:20:06.946Z