W. Zhao

发表

The Novel Gene Locus for Agenesis of Permanent Teeth (He-Zhao deficiency) Maps to Chromosome 10q11.2

Y. Zhao, W. Huang, W. Liu, 2001, Journal of dental research.

A Pro22Ser Mutation in NEFL Results in Charcot-Marie-Tooth Disease in a Chinese Family

W. Zhao, J. Ye, Q. Liang, 2020 .

Congenital absence of permanent teeth in a six-generation Chinese kindred.

W. Liu, S. Jiang, S. Li, 2000, American journal of medical genetics.

Medical complications in long-term survivors with X-linked myotubular myopathy.

Wei Zhao, G. Herman, M. Finegold, 1999, The Journal of pediatrics.

Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathy.

Wei Zhao, J. Mandel, G. Herman, 1997, Human molecular genetics.

Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.

J. Derry, A. Meindl, G. Herman, 1999, Nature genetics.

Creutzfeldt–Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP

X. Wang, B. Zhang, D. Wang, 2009, BMJ Case Reports.

Creutzfeldt–Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP

X. Wang, B. Zhang, D. Wang, 2007, Journal of Neurology, Neurosurgery & Psychiatry.

Mutations in NOTCH2 in patients with Hajdu–Cheney syndrome

P. Robey, R. Gafni, M. Seton, 2013, Osteoporosis International.