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1. Two novel mutations in ADAMTS13 in a Chinese boy with congenital thrombocytopenic purpura: a case report

   Authors:Ling Hou and Yue Du

   Content type:Case report

   20 March 2020

2. An eight-mRNA signature outperforms the lncRNA-based signature in predicting prognosis of patients with glioblastoma

   Authors:Zhenyu Gong, Fan Hong, Hongxiang Wang, Xu Zhang and Juxiang Chen

   Content type:Research article

   19 March 2020

3. Glutathione S-transferase M1 and T1 genes deletion polymorphisms and risk of developing essential hypertension: a case-control study in Burkina Faso population (West Africa)

   Authors:Herman Karim Sombié, Abel Pegdwendé Sorgho, Jonas Koudougou Kologo, Abdoul Karim Ouattara, Sakinata Yaméogo, Albert Théophane Yonli, Florencia Wendkuuni Djigma, Daméhan Tchelougou, Dogfounianalo Somda, Isabelle Touwendpoulimdé Kiendrébéogo, Prosper Bado, Bolni Marius Nagalo, Youssoufou Nagabila, Enagnon Tiémoko Herman Donald Adoko, Patrice Zabsonré, Hassanata Millogo…

   Content type:Research article

   19 March 2020

4. ABCG2 rs2231142 variant in hyperuricemia is modified by SLC2A9 and SLC22A12 polymorphisms and cardiovascular risk factors in an elderly community-dwelling population

   Authors:Jia Liu, Wei Yang, Yun Li, Zhanyun Wei and Xiaojuan Dan

   Content type:Research article

   17 March 2020

5. Novel variants in AP4B1 cause spastic tetraplegia, moderate psychomotor development delay and febrile seizures in a Chinese patient: a case report

   Authors:Wen-Cong Ruan, Jia Wang, Yong-Lin Yu, Yue-Ping Che, Li Ding, Chen-Xi Li, Xiao-Dong Wang and Hai-Feng Li

   Content type:Case report

   14 March 2020