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Genetic Testing and Molecular Biomarkers|January 31, 2012
Association of estrogen receptor alpha gene polymorphisms and risk of fractureGuoJun Wei, Meng Yao, YanSong Wang, et al.
Genetic Testing and Molecular Biomarkers|January 31, 2012
The mitochondrial DNA 9-bp deletion polymorphism is a risk factor for hepatocellular carcinoma in the Chinese populationYiqi Jin, Qiang Yu, Dayong Zhou, et al.
Genetic Testing and Molecular Biomarkers|March 1, 2012
Cytokine gene polymorphisms in the susceptibility to acute coronary syndromeBaddela M V Srikanth Babu, Bhomireddy Pulla Reddy, Vanacherla Hari Sai Priya, et al.
Genetic Testing and Molecular Biomarkers|May 17, 2012
Fibroblast growth factor receptor 4 polymorphisms are associated with coronary artery diseaseHao Chen, Jiabin Tong, Tong Zou, et al.
Genetic Testing and Molecular Biomarkers|June 7, 2012
Association of angiotensin I converting enzyme polymorphism as genetic risk factor in benign prostatic hyperplasia and prostate cancerMandana Hasanzad, Mohammad Samzadeh, Seyed Hamid Jamaldini, et al.
Genetic Testing and Molecular Biomarkers|July 1, 2017
Association Analysis of Single Nucleotide Polymorphisms in C1QTNF6, RAC2, and an Intergenic Region at 14q32.2 with Graves' Disease in Chinese Han PopulationXiao-Hong Zhang, Min Shen, Lin Liu, et al.
Genetic Testing and Molecular Biomarkers|August 11, 2018
Association of Desmin Gene Variant rs1058261 with Cardiovascular Disease, the TAMRISK StudyJaakko Piesanen, Tarja Kunnas, Seppo T Nikkari
Genetic Testing and Molecular Biomarkers|November 18, 2016
Genetic and Environmental Biomarkers Associated with Triglyceride Levels in Two Groups of Slovak WomenZuzana Danková, Lenka Vorobel'ová, Veronika Čerňanová, et al.
Genetic Testing and Molecular Biomarkers|February 11, 2010
Prevalence of mitochondrial tRNA gene mutations and their association with specific clinical phenotypes in patients with type 2 diabetes mellitus of CoimbatorePradeepa Duraisamy, Santhini Elango, Vijaya Padma Vishwanandha, et al.
Genetic Testing and Molecular Biomarkers|February 11, 2010
Clinical, cytogenetic, and molecular characterization of a girl with some clinical features of Down syndrome resulting from a pure partial trisomy 21q22.11-qter due to a de novo intrachromosomal duplicationAlicia Vaglio, Aubrey Milunsky, Andrea Quadrelli, et al.
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