Associated Papers
[Mutation analysis of FOXL2 gene and its structure protein in patients of blepharophimosis-ptosis-epicanthus inversus syndrome].
Lin LX et al.
[zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology, 2007
Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype.
Berry-Kravis EM et al.
American Journal of Respiratory and Critical Care Medicine, 2006
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