L. Hua

Rapid, accurate genotyping of the common −α4.2 thalassaemia deletion based on the use of denaturing HPLC

X. Xu, Q. Mo, H. Ou-yang, 2004, Journal of Clinical Pathology.

CYP 1 B 1 gene research of primary congenital glaucoma

Qing Sun, Guangqiang Feng, L. Hua, 2022 .

Carrier screening for α‐ and β‐thalassemia in pregnancy: the results of an 11‐year prospective program in Guangzhou Maternal and Neonatal hospital

Xiang-min Xu, C. Liao, Jian Li, 2005 .

A subgroup of microsatellite stable colorectal cancers has elevated mutation rates and different responses to alkylating and oxidising agents

J. Eshleman, A. Maitra, A. Parker, 2004, British Journal of Cancer.

Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital.

Xiang-min Xu, C. Liao, Jian Li, 2005, Prenatal diagnosis.

A reverse dot blot assay for the expanded screening of eleven Chinese G6PD mutations.

Xiaomei Lu, Ting Zhang, Siping Li, 2013, Clinica chimica acta; international journal of clinical chemistry.

Rapid, accurate genotyping of β‐thalassaemia mutations using a novel multiplex primer extension/denaturing high‐performance liquid chromatography assay

Xiang-min Xu, Grant Wu, Jim J. Zhu, 2003, British journal of haematology.