Publications
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Filters: Author is N.H. Yan [Clear All Filters]
“A novel frameshift deletion in the COL1A1 gene identified in a Chinese family with osteogenesis imperfecta”, vol. 14, pp. 15295-15300, 2015.
, “A novel mutation of PAX6 identified in a Chinese twin family with congenital aniridia complicated with nystagmus”, vol. 13, pp. 8679-8685, 2014.
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