Browsing by Author Qin, Yaping
Showing results 1 to 5 of 5
Issue Date |
Title |
Author(s) |
2015 |
Eleven novel mutations of the BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease in the Chinese population: Report on eight cases |
Li, Xiyuan;Ding, Yuan;Liu, Yupeng;Ma, Yanyan;Song, Jinqing;Wang, Qiao;Li, Mengqiu;Qin, Yaping;Yang, Yanling |
2015 |
The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1 |
Wang, Qiao;Li, Xiyuan;Ding, Yuan;Liu, Yupeng;Qin, Yaping;Yang, Yanling |
2016 |
Seven novel mutations of the SMPD1 gene in four Chinese patients with Niemann-Pick disease type A and prenatal diagnosis for four fetuses |
Ding, Yuan;Li, Xiyuan;Liu, Yupeng;Hua, Ying;Song, Jinqing;Wang, Liwen;Li, Mengqiu;Qin, Yaping;Yang, Yanling |
2015 |
Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses |
Li, Xiyuan;Ding, Yuan;Liu, Yupeng;Zhang, Yao;Song, Jinqing;Wang, Qiao;Li, Mengqiu;Qin, Yaping;Huang, Shangzhi;Yang, Yanling |
2016 |
succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses (vol 574, pg 41, 2015) |
Li, Xiyuan;Ding, Yuan;Liu, Yupeng;Zhang, Yao;Song, Jinqing;Wang, Qiao;Li, Mengqiu;Qin, Yaping;Huang, Shangzhi;Yang, Yanling |