Ghaedi, H., Ramsheh, S. M., Omidvar, M. E., Labbaf, A., Alehabib, E., Akbari, S., . . . Darvish, H. (2019). Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome. Genes Dis.
Citação norma ChicagoGhaedi, Hamid, Samira Molaei Ramsheh, Maryam Erfanian Omidvar, Afsaneh Labbaf, Elham Alehabib, Sanaz Akbari, Fatemeh Pourfatemi, and Hossein Darvish. "Whole-exome Sequencing Identified a Novel Mutation of MLH1 in an Extended Family With Lynch Syndrome." Genes Dis 2019.
MLA citiranjeGhaedi, Hamid, et al. "Whole-exome Sequencing Identified a Novel Mutation of MLH1 in an Extended Family With Lynch Syndrome." Genes Dis 2019.
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