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BMC Medical Genomics|May 25, 2022
Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutationPing Gu, Guojian Wang, Xue Gao, et al.
BMC Medical Genomics|May 21, 2022
Multiple metastases of androgen indifferent prostate cancer in the urinary tract: two case reports and a literature reviewTsukasa Masuda, Takeo Kosaka, Kohei Nakamura, et al.
BMC Medical Genomics|July 4, 2021
Hypodiploidy in a pediatric patient of T-cell acute lymphoblastic leukemia: a case reportMartyna Stefaniak, Gabriela Ręka, Joanna Zawitkowska, et al.
BMC Medical Genomics|July 10, 2021
Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patientsJuan Xiong, Haolin Duan, Shimeng Chen, et al.
BMC Medical Genomics|July 1, 2021
Novel homozygous mutations in Pakistani families with Charcot-Marie-Tooth diseaseSumaira Kanwal, Yu JIn Choi, Si On Lim, et al.
BMC Medical Genomics|June 5, 2021
A novel mutation of COL2A1 in a large Chinese family with avascular necrosis of the femoral headZeng Zhang, Kechao Zhu, Huiyong Dai, et al.
BMC Medical Genomics|January 8, 2021
The Genomics of Opioid Addiction Longitudinal Study (GOALS): study design for a prospective evaluation of genetic and non-genetic factors for development of and recovery from opioid use disorderJessica Heil, Stefan Zajic, Emily Albertson, et al.
BMC Medical Genomics|June 9, 2021
A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > AYu Sui, Yongping Lu, Meina Lin, et al.
BMC Medical Genomics|June 10, 2021
Genome-wide analysis of retinal transcriptome reveals common genetic network underlying perception of contrast and optical defocus detectionTatiana V Tkatchenko, Andrei V Tkatchenko
BMC Medical Genomics|June 12, 2021
A blood RNA transcriptome signature for COVID-19Philip Kam Weng Kwan, Gail B Cross, Claire M Naftalin, et al.
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