Huakun Shangguan

Phenotypes of Cornelia de Lange syndrome caused by non-cohesion genes: Novel variants and literature review

Ruimin Chen, Huakun Shangguan, Ruimin Chen, 2022, Frontiers in Pediatrics.

Kabuki syndrome: novel pathogenic variants, new phenotypes and review of literature

C. Gong, B. Cao, C. Su, 2019, Orphanet Journal of Rare Diseases.

Clinical and genetic analysis of two Chinese families with vitamin D-dependent rickets type IA and follow-up

Xin Yuan, Xiang-quan Lin, Xiao-hong Yang, 2020, Orphanet Journal of Rare Diseases.

Wiedemann-Steiner syndrome caused by novel mutation of KMT2A gene: one case report and literature review

Yiping Shen, Xuyun Hu, Xin Yuan, 2019 .

Associations of Obesity With Growth and Puberty in Children: A Cross-Sectional Study in Fuzhou, China

Wenyong Wu, Xin Yuan, Xiang-quan Lin, 2023, International Journal of Public Health.