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BMC Medical Genetics | Home page

BMC Medical Genetics

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1. Content Type:Research Article

     |  5 July 2019

   Interaction between mitochondrial NADH dehydrogenase subunit-2 5178 C > A and clinical risk factors on the susceptibility of essential hypertension in Chinese population

   Authors:Xi Chen, Xiang-Yu He, Chao Zhu, Yusong Zhang, Zongbin Li, Yuqi Liu, Yuxiao Zhang, Tong Yin and Yang Li
2. Content Type:Case Report

     |  5 July 2019

   Identification of a novel RPS26 nonsense mutation in a Chinese Diamond-Blackfan Anemia patient

   Authors:Xiaodong Shi, Xiaolan Huang, Yu Zhang and Xiaodai Cui
3. Content Type:Case Report

     |  4 July 2019

   Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

   Authors:Salma M. Wakil, Safa Alhissi, Haya Al Dossari, Ayesha Alqahtani, Sherin Shibin, Brahim T. Melaiki, Josef Finsterer, Amal Al-Hashem, Saeed Bohlega and Anas M. Alazami
4. Content Type:Research Article

     |  2 July 2019

   SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct

   Authors:Janet R. Chao, Parna Chattaraj, Tina Munjal, Keiji Honda, Kelly A. King, Christopher K. Zalewski, Wade W. Chien, Carmen C. Brewer and Andrew J. Griffith
5. Content Type:Research Article

     |  1 July 2019

   Overexpression of MicroRNA-148b-3p stimulates osteogenesis of human bone marrow-derived mesenchymal stem cells: the role of MicroRNA-148b-3p in osteogenesis

   Authors:Samaneh Mollazadeh, Bibi Sedigheh Fazly Bazzaz, Vajiheh Neshati, Antoine A. F. de Vries, Hojjat Naderi-Meshkin, Majid Mojarad, Mahdi Mirahmadi, Zeinab Neshati and Mohammad Amin Kerachian