Publications
Found 6 results
Filters: Author is N. Fan [Clear All Filters]
, ,
“A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome”, vol. 14, pp. 4125-4132, 2015.
, “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.
, “A novel NF1 frame-shift mutation (c.702_703delGT) in a Chinese family with neurofibromatosis type 1”, vol. 13, pp. 5395-5404, 2014.
,