X. Xu

发表

Development and validation of a ζ-globin-specific ELISA for carrier screening of the (−−SEA) α thalassaemia deletion

N. Fu, L. Tang, P. Zhu, 2009, Journal of Clinical Pathology.

The prevalence and spectrum of alpha and beta thalassaemia in Guangdong Province: implications for the future health burden and population screening.

Y. Li, G. Luo, C. Liao, 2004, Journal of clinical pathology.

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.

Antenatal screening and fetal diagnosis of β-thalassemia in a Chinese population: prevalence of the β-thalassemia trait in the Guangzhou area of China

C. Liao, Jian Li, X. Xu, 1996, Human Genetics.

Direct genotyping and prenatal diagnosis of beta-thalassemia in Chinese by polymerase chain reaction mediated restriction fragment length polymorphism method.

J. Z. Zhang, X. Xu, Q. Xu, 1993, Clinical biochemistry.

Molecular study and prenatal diagnosis of alpha- and beta-thalassemias in Chinese.

T. Ko, X. Xu, 1998, Journal of the Formosan Medical Association = Taiwan yi zhi.

[Molecular screening and prenatal diagnosis of the deletional alpha-thalassemia by polymerase chain reaction amplification].

J. Li, X. Cai, X. Xu, 1994, Zhonghua yi xue za zhi.

Rapid PCR detection of the Hb constant spring mutation using an artificial-restriction fragment length polymorphism.

J. Z. Zhang, X. Xu, S. Li, 1994, Hemoglobin.