Xinhuo Guo

Circular RNA hsa_circ_0007990 as a blood biomarker for unruptured intracranial aneurysm with aneurysm wall enhancement

Peiyun Chen, Chun Xiang, Xiaobei Wu, 2022, Frontiers in Immunology.

Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm.

J. Bieker, C. Westhoff, S. Seshan, 2013, Blood Cells, Molecules & Diseases.

Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott–Aldrich syndrome

F. Ma, Xin Ji, Xinhuo Guo, 2022, Orphanet journal of rare diseases.