A novel FOXL2 mutation in a Chinese family with...

Human Genome Variation 2015 / 3 Vol. 2

A novel FOXL2 mutation in a Chinese family with blepharophimosis, ptosis, epicanthus inversus syndrome

Tan, Hu, Yang, Pu, Li, Haoxian, Pan, Qian, Liang, Desheng, Wu, Lingqian
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Volume:
2
Language:
english
Journal:
Human Genome Variation
DOI:
10.1038/hgv.2015.8
Date:
March, 2015
File:
PDF, 634 KB
english, 2015
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