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1. The genome-wide supported CACNA1C gene polymorphisms and the risk of schizophrenia: an updated meta-analysis

   Authors:Yong-ping Liu, Xue Wu, Xi Xia, Jun Yao and Bao-jie Wang

   Content type:Research article

    

   8 August 2020

2. Dual molecular diagnosis of tricho-rhino-phalangeal syndrome type I and Okur-Chung neurodevelopmental syndrome in one Chinese patient: a case report

   Authors:Shanshan Xu, Qun Lian, Jinzhun Wu, Lingli Li and Jia Song

   Content type:Case report

    

   3 August 2020

3. Association studies of dopamine synthesis and metabolism genes with multiple phenotypes of heroin dependence

   Authors:Yunxiao Li, Yongsheng Zhu, Jianghua Lai, Xugang Shi, Yuanyuan Chen, Jinyu Zhang and Shuguang Wei

   Content type:Research article

    

   31 July 2020

4. Clinical, biochemical, and genetic analysis of a Chinese Han pedigree with holocarboxylase synthetase deficiency: a case report

   Authors:Zhenzhu Zheng, Gaopin Yuan, Minyan Zheng, Yiming Lin, Faming Zheng, Mengyi Jiang, Lin Zhu and Qingliu Fu

   Content type:Case report

    

   29 July 2020

5. A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss

   Authors:Mingming Wang, Yicui Zhou, Fengguo Zhang, Zhaomin Fan, Xiaohui Bai and Haibo Wang

   Content type:Research article

    

   25 July 2020