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BMC Medical Genetics

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1. A case report and mechanism analysis of a normal phenotype mosaic 47, XXY complicated by paternal iUPD (9) who had a normal PGD result

   Authors:Dan Li, Yun Wang, Nan Zhao, Liang Chang, Ping Liu, Chan Tian and Jie Qiao

   Content type:Case report

   7 November 2019

2. Screening and computational analysis of colorectal associated non-synonymous polymorphism in CTNNB1 gene in Pakistani population

   Authors:Suhail Razak, Nousheen Bibi, Javid Ahmad Dar, Tayyaba Afsar, Ali Almajwal, Zahida Parveen and Sarwat Jahan

   Content type:Research article

   7 November 2019

3. Association of high sensitive C-reactive protein with coronary heart disease: a Mendelian randomization study

   Authors:Qian Zhuang, Chong Shen, Yanchun Chen, Xianghai Zhao, Pengfei Wei, Junxiang Sun, Yanni Ji, Xiaotian Chen and Song Yang

   Content type:Research article

   6 November 2019

4. Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling

   Authors:Cong Ma, Lv Liu, Fang-Na Wang, Hai-Shen Tian, Yan Luo, Rong Yu, Liang-Liang Fan and Ya-Li Li

   Content type:Case report

   6 November 2019

5. Associations of BAFF rs2893321 polymorphisms with myasthenia gravis susceptibility

   Authors:Hui Deng, Jianjian Wang, Xiaotong Kong, Huixue Zhang, Tianfeng Wang, Wenqi Tian, Tingting Yi and Lihua Wang

   Content type:Research article

   30 October 2019