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BMC Medical Genomics|December 22, 2023
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathySerwa Ghasemi, Mohammad Mahdavi, Majid Maleki, et al.
BMC Medical Genomics|December 15, 2023
An FGFR2 mutation as the potential cause of a new phenotype including early-onset osteoporosis and bone fractures: a case reportIlya S Dantsev, Mariia A Parfenenko, Gulnara M Radzhabova, et al.
BMC Medical Genomics|December 13, 2023
BMC3PM: bioinformatics multidrug combination protocol for personalized precision medicine and its application in cancer treatmentMajid Mokhtari, Samane Khoshbakht, Mohammad Esmaeil Akbari, et al.
BMC Medical Genomics|November 29, 2023
A novel necroptosis signature for predicting survival in lung adenocarcinomaKui Zang, Min Wang, Xingxing Zhu, et al.
BMC Medical Genomics|December 1, 2023
Integrated analysis of microRNA and mRNA expression profiles in PreeclampsiaZepeng Ping, Ying Feng, Ying Lu, et al.
BMC Medical Genomics|December 2, 2023
Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?Cinthia Aguilera, Anna Esteve-Garcia, Carlos Casasnovas, et al.
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