Embryonic Alternative Intron Amalgamation Syndrome

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A syndrome asserted during the formation of an embryo where evolutionary holdovers become combined into the whole genome of the embryo before differentiation of cellular function from the zygote. There are two kinds stable and unstable, the genetic structures have traditionally not been recombinant with introns in a stable way. An unstable syndrome will cause significant birth defects or a fetus to become unviable at the earliest stages.

When this syndrome is exhibited in a stable state, the introns are recombined in an alternative (i.e. atypical) way which genetically combined into an amalgam of biologically compatible attributes. In a stable exhibit of this syndrome, the stem cells differentiate into an entirely stable life form. This organism will exhibit physical, mental, or other biological characteristics of multiple species whose genetic sequences are present as introns in the typical organism but are now exons which inform cellular growth and function throughout the orgnism.