HuGE Literature Finder
Records 1-1
Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform.
BMC medical genetics 2013 14 (1): 112. Martins Fábio Tadeu Arrojo, Ramos Priscila Zonzini, Svidnicki Maria Carolina Costa Melo, Castilho Arthur Menino, Sartorato Edi Lúc |
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- Page last updated:Feb 24, 2021
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