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However, the membrane based clones are not a versatile tool for validation of those candidate makers.
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The number of clones was not associated with haemoglobin levels.
The clones affiliated with δ-Proteobacteria decreased to 1.3% while Firmicutes clones were not detectable any more.
The remaining clones were not further analyzed.
Four boPAG genes, boPAGs- 7, 13, 14 and - 22, previously described based on cDNA cloning, were not represented in the build.
Noteworthy, the BAC fragment contained in this clone is not evolutionarily conserved based on current annotations and detection methods (UCSC genome browser [27], Vertebrate Multiz Alignment & PhastCons Conservation [28],).
It said cloning was not unfair because the genetic match is not 100 per cent and much of a horse's performance is based on training, conditions, and the rider.
Cloning is not unnatural.
Therapeutic cloning is not a new idea.
Across the Atlantic, therapeutic cloning is not even being discussed.
However, A-clones were not consistently socially dominant over B-clones.
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