Bo Cai

Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network

S. Pandya, K. Mathews, J. Howard, 2022, Neuromuscular Disorders.

The genotype and phenotype of chromosome 18p deletion syndrome

R. Qiang, Wen Zhai, Xiaobin Wang, 2021, Medicine.

Unexpected DMD Gene Mutations Detected by CMA and CNV-seq in amniotic Fluid and Aborted Fetus Samples

Lihui Yang, R. Qiang, Wen Zhai, 2021 .

Sources of variation in estimates of Duchenne and Becker muscular dystrophy prevalence in the United States

J. Howard, L. Ouyang, S. McDermott, 2023, Orphanet Journal of Rare Diseases.