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Items: 3

1.
Oculomotor Deficits in Aryl Hydrocarbon Receptor Null Mouse
Aline Chevallier, Antoine Mialot, Jean-Maurice Petit, Pedro Fernandez-Salguero, Robert Barouki, Xavier Coumoul, Mathieu Beraneck
PLoS One. 2013; 8(1): e53520. Published online 2013 Jan 3. doi: 10.1371/journal.pone.0053520
PMCID:
PMC3536739
AbstractArticlePDF–4.6M
2.
Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families
Arif O. Khan, Jameela Shinwari, Aisha Omar, Latifa Al-Sharif, Dania S. Khalil, Mohammed Alanazi, Abdullah Al-Amri, Nada Al Tassan
Mol Vis. 2011; 17: 218–224. Published online 2011 Jan 20.
PMCID:
PMC3025099
AbstractArticlePDF–881K
3.
CONGENITAL ABNORMALITIES OF CRANIAL NERVE DEVELOPMENT: OVERVIEW, MOLECULAR MECHANISMS, AND FURTHER EVIDENCE OF HETEROGENEITY AND COMPLEXITY OF SYNDROMES WITH CONGENITAL LIMITATION OF EYE MOVEMENTS
Elias I Traboulsi
Trans Am Ophthalmol Soc. 2004 Dec; 102: 373–390.
PMCID:
PMC1280110
AbstractArticlePDF–4.1M

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