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European Journal of Medical Genetics|June 24, 2019
Molecular genetic study of 59 Chinese Oculocutaneous albinism familiesDan Luo, Siyuan Linpeng, Lanlan Zeng, et al.
Human Genome Variation|April 16, 2016
A novel FOXL2 mutation in a Chinese family with blepharophimosis, ptosis, epicanthus inversus syndromeHu Tan, Pu Yang, Haoxian Li, et al.
Familial Cancer|February 11, 2017
A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case reportHu Tan, Xianda Wei, Pu Yang, et al.
Gene|May 20, 2018
Deficiency in GnRH receptor trafficking due to a novel homozygous mutation causes idiopathic hypogonadotropic hypogonadism in three prepubertal siblingsRui Zhang, Siyuan Linpeng, Zhuo Li, et al.
Molecular Medicine Reports|May 7, 2019
Novel variants in the KERA gene cause autosomal recessive cornea plana in a Chinese family: A case reportChengzi Huang, Xigui Long, Can Peng, et al.
International Heart Journal|August 14, 2018
Three Novel Mutations in FBN1 and TGFBR2 in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and DissectionsYingxi Cao, Hu Tan, Zhuo Li, et al.
American Journal of Translational Research|June 28, 2016
Advanced glycation endproducts induce apoptosis of endothelial progenitor cells by activating receptor RAGE and NADPH oxidase/JNK signaling axisJianfei Chen, Jun Jing, Shiyong Yu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2020
Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencingHu Tan, Yinong Xie, Fei Chen, et al.
Seizure|January 17, 2020
Posterior reversible encephalopathy syndrome in preeclampsia and eclampsia: The role of hypomagnesemiaXiaobo Fang, Haibin Wang, Zifan Liu, et al.
Nephrology (Carlton, Vic.)|May 14, 2024
Multiple myeloma complicated with light chain cast nephropathy with focal amyloidosis: A case reportYicao He, Zhijuan Hua, Hu Tan, et al.
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