Excision repair exon fluorescence in situ hybridization (fish) human genome project insertion sequence (is) a. the portion of a eukaryotic gene that will be transcribed and then translated into protein; interrupted by introns b. the now-completed undertaking to sequence the human genome c. a procedure using a fluorescence-labeled probe to detect specific nucleotide sequences within intact cells attached to a microscopic slide d. short piece of dna able to move from one site on a dna molecule to another; simplest type of transposable element e. mechanism of dna repair in which a fragment of single-stranded dna containing mismatched bases is removed and replaced

Excision repair is correctly matched with E. It is a DNA repair mechanism in which a single stranded DNA fragment comprising mismatched bases is withdrawn and substituted.  

Exon is correctly matched with A. It is a part of a eukaryotic gene, which will be transcribed and then translated into protein, and is interrupted by proteins.  

FISH or fluorescence in situ hybridization is correctly matched with C. It is a process in which a fluorescence-labeled probe is used to determine particular sequences of nucleotide within the intact cells associated with a microscopic slide.  

Human genome project is correctly matched with B. It is the presently completed undertaking to sequence the genome of human beings.  

Insertion sequence is correctly matched with D. It is a short fragment of DNA that possesses the tendency to move from one location on the DNA molecule to another. It is a basic kind of transposable element.

a and b

this is true, assuming that the allele is completely recessive and incomplete dominance is not a factor.