- 期刊
Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency
延伸閱讀
- 吳曉涵、張璧月、盧章智（2012）。The Importance of Detection of CYP2C19 Genetic Polymorphism in Clinical Pharmacogenetics。Journal of Biomedical & Laboratory Sciences，24(4)，109-114。https://doi.org/10.30046/JBLS.201212.0001
- 陳鵬文（2003）。Genetic Polymorphisms of Inflammatory Cytokine Genes and Chronic Obstructive Pulmonary Disease〔碩士論文，高雄醫學大學〕。華藝線上圖書館。https://www.airitilibrary.com/Article/Detail?DocID=U0011-0707200816054464
- 賀筠婷（2012）。CYP2C19 Genetic Polymorphisms in Relation to Voriconazole Concentration and Adverse Drug Reactions〔碩士論文，國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2012.03269
- Lee, F. H. (2005). Studies on The Function of Two Hepatocellular Carcinoma Candidate Genes--Cyclase-associated Protein 1 and Cofilin [master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2005.02071
- Tsai, C. H., Lin, W. D., Tsai, F. J., Peng, C. T., & Wu, J. Y. (2001). Pitfalls of PCR-based Genotyping in Patients with 21-hydroxylase Deficiency. Acta Paediatrica Taiwanica, 42(3), 145-150. https://doi.org/10.7097/APT.200106.0145