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	1.	Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome. [electronic resource] by Or, Siu-fong June Tong, Ming-for Tony Lo, Fai-man Ivan Lam, Tak-sum Stephen Producer: 20060316 In: Chinese medical journal vol. 119 Availability: No items available. Save to lists Add to cart (remove)
	2.	Maternal somatic mosaicism of FOXF1 mutation causes recurrent alveolar capillary dysplasia with misalignment of pulmonary veins in siblings. [electronic resource] by Luk, Ho Ming Tang, Tao Choy, Kwong Wai Richard Tong, Ming For Tony Wong, On Kit Lo, Fai Man Ivan Producer: 20180129 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome. [electronic resource] by Or, Siu-Fong June Tong, Ming-for Tony Lo, Fai-Man Ivan Law, Chi-Wai Miu, Ting-Yat Trochet, Delphine Lam, Tak-Sum Stephen Producer: 20061213 In: Chinese medical journal vol. 119 Availability: No items available. Save to lists Add to cart (remove)

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