Jia-wei Wang

Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta

Asan, X. Xing, W. Xia, 2016, Journal of Human Genetics.

Familial Early-Onset Paget’s Disease of Bone Associated with a Novel hnRNPA2B1 Mutation

Asan, X. Qi, X. Xing, 2017, Calcified Tissue International.

Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid

Asan, X. Xing, W. Xia, 2016, Journal of Human Genetics.

A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.

Asan, X. Xing, W. Xia, 2016, Clinica chimica acta; international journal of clinical chemistry.

Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.

X. Xing, W. Xia, Yan Jiang, 2016, Clinica chimica acta; international journal of clinical chemistry.

Targeted Genes Sequencing Identified a Novel 15 bp Deletion on GJA8 in a Chinese Family with Autosomal Dominant Congenital Cataracts

Asan, X. Yi, Ling Yang, 2016, Chinese medical journal.

Familial Early-Onset Paget’s Disease of Bone Associated with a Novel hnRNPA2B1 Mutation

Asan, X. Xing, J. Mao, 2017, Calcified Tissue International.