Yan Li

Association between SMN2 methylation and disease severity in Chinese children with spinal muscular atrophy

Yu-wei Jin, Y. Qu, Hong Wang, 2016, Journal of Zhejiang University-SCIENCE B.

Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene

Yu-wei Jin, Y. Qu, Hong Wang, 2014, Journal of Zhejiang University SCIENCE B.

Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene

Y. Qu, Hong Wang, J. Bai, 2014, Journal of Zhejiang University SCIENCE B.

X-linked ichthyosis and Crigler-Najjar syndrome I: Coexistence in a male patient with two copy number variable regions of 2q37.1 and Xp22.3

Y. Qu, Hong Wang, J. Bai, 2015, Molecular medicine reports.

Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.

C. Eng, R. Pilarski, M. Pezzolesi, 2006, American journal of human genetics.

Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy.

Y. Qu, Hong Wang, J. Bai, 2016, The Journal of molecular diagnostics : JMD.

Association between SMN2 methylation and disease severity in Chinese children with spinal muscular atrophy

Y. Qu, Hong Wang, J. Bai, 2016, Journal of Zhejiang University-SCIENCE B.

No point mutation but a codon 31ser-->arg polymorphism of the WAF-1/CIP-1/p21 tumor suppressor gene in nasopharyngeal carcinoma (NPC): the polymorphism distinguishes Caucasians from Chinese.

R. Hayes, A. Hildesheim, Y. Sun, 1995, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.