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pro vyhledávání: '"Alfawaz, Shurog Abdulrahman"'
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Alfawaz, Shurog Abdulrahman
An evolution in methods of identifying the causal mutations and candidate genes for Mendelian disorders has occurred recently. Though several studies have reported the causative mutations in non syndromic tooth agenesis, there are only two reports on
Externí odkaz:
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667200
