Yan Lu

NEK1 and GRN mutations coexist in a sporadic Chinese Hui descent ALS patient

Kang Zhang, Yan Lu, Jianhong Chen, 2020, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Case report: A novel mosaic nonsense mutation of PCDH19 in a Chinese male with febrile epilepsy

Yan Lu, Jin Han, Ruibin Huang, 2022, Frontiers in Neurology.

Case Report: A Paternal 20q13.2-q13.32 Deletion Patient With Growth Retardation Improved by Growth Hormone

Y. Li, J. Wen, X. Shao, 2022, Frontiers in Genetics.

Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysis

C. Liao, T. Lei, F. Fu, 2022, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus

C. Liao, Dongzhi Li, F. Fu, 2022, Frontiers in Genetics.