Revision history of "Whole exome sequencing within silico and also welldesigned research look at the connection with the GJB2 mutation sCys169Tyr along with deaf ness as well as advise a function to the TMEM59 gene within the hearing method"

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  • (cur | prev) 08:24, 23 April 2024‎ Clubbronze93 (Talk | contribs)‎ . . (3,651 bytes) (+3,651)‎ . . (Created page with "The particular positioning of 5 HAs had been examined pertaining to red (RBC, Hb, MCV, RET), white (WBC, NE, Of all, MO, . e . o, BA, IG), and platelet (PLT) sequence guidelin...")
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