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- {{r|Space Quest V: The Next Mutation}}516 bytes (78 words) - 09:06, 7 April 2010
- {{r|Mutation}}836 bytes (104 words) - 06:18, 23 May 2010
- {{r|Mutation}}606 bytes (81 words) - 21:04, 11 January 2010
- {{r|Mutation}}715 bytes (95 words) - 17:20, 11 January 2010
- {{r|Mutation}}643 bytes (89 words) - 05:10, 9 June 2009
- {{r|Mutation}}728 bytes (86 words) - 21:08, 17 April 2011
- {{r|Mutation}}869 bytes (109 words) - 16:26, 11 January 2010
- {{r|Mutation}}791 bytes (103 words) - 07:44, 8 January 2010
- {{r|Mutation}}831 bytes (112 words) - 19:43, 11 January 2010
- {{r|Mutation}}855 bytes (110 words) - 21:04, 11 January 2010
- ...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers886 bytes (120 words) - 11:57, 24 October 2010
- Some used "[[mutation]]" to refer to variations with low allele frequency. ...if a different polypeptide sequence is produced they are ''[[nonsynonymous mutation|nonsynonymous]]''.7 KB (957 words) - 10:47, 30 March 2010
- {{r|Mutation}}1,006 bytes (130 words) - 10:50, 11 January 2010
- ...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers965 bytes (129 words) - 22:06, 22 August 2010
- ...s'' is the inability to respond to vaopressin, (for instance if there is a mutation affecting the V2 vasopressin receptor) and cannot be treated in this way. ...hypothalamic diabetes insipidus is most commonly a consequence of a point mutation in the vasopressin gene, usually in the region coding for vasopressin-assoc4 KB (506 words) - 09:39, 24 July 2011
- ...//www.blackwellpublishing.com/ridley/classictexts/wright.asp "The roles of mutation, inbreeding, crossbreeding and selection in evolution"] ''Proc. 6th Int. Co1 KB (149 words) - 23:10, 15 February 2009
- ...ooks at how large scale changes may be caused by evolutionary mechanisms—[[mutation]], [[migration]], [[genetic drift]], and [[natural selection]].<ref>[http:/1 KB (169 words) - 06:31, 31 May 2009
- Auto-populated based on [[Special:WhatLinksHere/Mutation]]. Needs checking by a human.1 KB (167 words) - 18:44, 11 January 2010
- ...h [[natural selection]] and other [[evolution]]ary processes acts. Without mutation, there are no new [[gene]]s, no new [[allele]]s and, eventually, no evoluti ...], where mutations occur up to 100 times more frequently than the normal [[mutation rate]]. A hotspot can be at an unusual base, e.g., 5-methylcytosine.13 KB (2,019 words) - 00:14, 11 November 2007
- ...indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Rom ...siology involving the [[voltage-gated potassium channel]]. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).."<4 KB (593 words) - 10:17, 25 March 2011