J. Wang

发表

A novel CFTR frame-shift mutation, 935delA, in two Hispanic cystic fibrosis patients.

L. Wong, C. M. Bowman, J. Wang, 2000, Molecular genetics and metabolism.

Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum

M. Hua, D. Stephenson, Ming-Kai Pan, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two families

P. Scambler, W. Reardon, R. Winter, 1999, European Journal of Pediatrics.

Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism

Yiping Shen, X. Fan, H. Zheng, 2015, Journal of Endocrinological Investigation.

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome

W. Craigen, M. Shinawi, A. El-Hattab, 2017, Clinical genetics.

HMBS Mutations in Chinese Patients with Acute Intermittent Porphyria

D. Stephenson, C. Yang, M. Lan, 2008, Annals of human genetics.

[Analysis of four carnitine-acylcarnitine translocase deficiency cases caused by homozygous mutation of SLC25A20 c.199-10T> G].

Q. Zhang, X. Fan, C. Li, 2018, Zhonghua er ke za zhi = Chinese journal of pediatrics.

A novel mutation in the CFTR gene correlates with severe clinical phenotype in seven Hispanic patients

L. Wong, J. Wang, M. Bowman, 2000, Journal of medical genetics.

Fibrillin mutations in the Marfan syndrome

C. Price, M. Godfrey, J. Wang, 1994 .