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1. A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case report

   Authors:Hai-rong Wang, Yan-qiu Liu, Xue-lian He, Jun Sun, Fan-wei Zeng, Cheng-bin Yan, Hao Li, Shu-yang Gao and Yun Yang

   Content type:Case report

    

   20 August 2020

2. Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report

   Authors:D. Hettiarachchi, Hetalkumar Panchal, P. S. Lai and V. H. W. Dissanayake

   Content type:Case report

    

   20 August 2020

3. Association of PNPLA3 rs738409 G/C gene polymorphism with nonalcoholic fatty liver disease in children: a meta-analysis

   Authors:Shan Tang, Jing Zhang, Ting Ting Mei, Hai Qing Guo, Xin Huan Wei, Wen Yan Zhang, Ya Li Liu, Shan Liang, Zuo Peng Fan, Li Xia Ma, Wei Lin, Yi Rong Liu, Li Xia Qiu and Hai Bin Yu

   Content type:Research article

    

   18 August 2020

4. Case report expanding the germline AXIN2- related phenotype to include olfactory neuroblastoma and gastric adenoma

   Authors:Sarah K. Macklin- Mantia, Stephanie L. Hines, Kaisorn L. Chaichana, Angela M. Donaldson, Stephen L. Ko, Qihui Zhai, Niloy Jewel Samadder and Douglas L. Riegert-Johnson

   Content type:Case report

    

   17 August 2020

5. Association of MC4R (rs17782313) with diabetes and cardiovascular disease in Korean men and women

   Authors:Jae Woong Sull, Gitae Kim and Sun Ha Jee

   Content type:Research article

    

   17 August 2020