Results 101 to 110 of about 330 (127)

[Research advances on mechanism and lesion location of vertical nystagmus]. [PDF]

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi, 2020
Chen G, Zhang C, Gao W, Fan H, Huang F, Fan H, Wang B.   +6 more
europepmc   +1 more source

[Pathogenic mechanisms of Leber hereditary optic neuropathy caused by m.3472T>C mutation]. [PDF]

Zhejiang Da Xue Xue Bao Yi Xue Ban
Zhang H, Shan W, Yasheng M, Guan M.
europepmc   +1 more source

[Correlation of serum ferredoxin 1 and lipoic acid levels with severity of coronary artery disease]. [PDF]

Nan Fang Yi Ke Da Xue Xue Bao
Wei T, Ding Y, Zhang J, Li J, Zhang H, Kang P, Zhang N.   +6 more
europepmc   +1 more source

[Pedigree analysis of novel missense mutations causing hereditary coagulation factor Ⅴ deficiency]. [PDF]

Zhonghua Xue Ye Xue Za Zhi
Qin LY, Chen Y, Hou LL, Jin YH, Lu YF, Zhang K, Wang MS.   +6 more
europepmc   +1 more source

Correction: Chinese Social Media Reaction to Information about 42 Notifiable Infectious Diseases. [PDF]

PLoS One, 2015
PLOS ONE Staff.
europepmc   +1 more source

[Late-onset hereditary hearing loss caused by TMPRSS3 compound heterozygous mutations]. [PDF]

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
Wang Y, Liang Y, Huang B, Cen X, Huang L, Chen K.   +5 more
europepmc   +1 more source

[Alpers-Huttenlocher syndrome caused by a novel compound heterozygous mutation of POLG gene: a case report]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi, 2017
Zhang YF, Wang JT, Gao JB, Lyu YY, Liang JM, Jia FY, Chen YB, Hao YP.   +7 more
europepmc   +1 more source

HDAC6-mediated deacetylation of FLOT2 maintains stability and tumorigenic function of FLOT2 in nasopharyngeal carcinoma. [PDF]

Zhong Nan Da Xue Xue Bao Yi Xue Ban
Luo C, Wen B, Liu J, Yang W.
europepmc   +1 more source

[Efficiency of 27-plex single nucleotide polymorphism multiplex system for ancestry inference in different populations]. [PDF]

Nan Fang Yi Ke Da Xue Xue Bao, 2016
Feng XL, Sun QF, Liu H, Wei YL, DU WA, Li CX, Chen L, Liu C.   +7 more
europepmc   +1 more source

[Genetic and phenotypic analysis of MYO15A rare variants associated with autosomal recessive hearing loss]. [PDF]

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
Lin Y, Xu J, Yang T.
europepmc   +1 more source