Open Access
| Issue |
J Oral Med Oral Surg
Volume 25, Number 1, 2019
|
|
|---|---|---|
| Article Number | 5 | |
| Number of page(s) | 2 | |
| Section | Cas clinique / Short case report | |
| DOI | https://doi.org/10.1051/mbcb/2018033 | |
| Published online | 22 February 2019 | |
- Morisada N, Nozu K, Iijima K. Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan. Pediatr 2014;56:309–314. [Google Scholar]
- Li G, Shen Q, Sun L, Liu H, An Y, Xu H. A de novo and novel mutation in the EYA1 gene in a Chinese child with branchio-oto-renal syndrome. Intractable Rare Dis Res 2018;7:42–45. [CrossRef] [PubMed] [Google Scholar]
- Xu PX, Adams J, Peters H, Brown MC, Heaney S, Maas R. Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat Genet 1999;23:113–117. [Google Scholar]
- Smith RJ. Branchiootorenal spectrum disorders. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993 [cited 2018 May 17]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1380/ [Google Scholar]
- Ou Z, Martin DM, Bedoyan JK, Cooper ML, Chinault AC, Stankiewicz P, et al. Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement. Am J Med Genet A 2008;146A(19):2480–2489. [Google Scholar]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.