Answer:
The correct answer is - option C.
Explanation:
CFTR is a short form of cystic fibrosis transmembrane conductance regulator protein which is caused by a recessive mutation in this protein. This mutation results in the accumulation of mucus in secretory organs.
As the disease is a recessive disease, for the mutant phenotype to expressed both copies of the allele required to be recessive.
The mother is negative for the CFTR. Hence, she will not transfer the mutant allele to her child So, the child would have a wild-type phenotype even if the father having two copies of recessive allele.
Thus, the correct answer is - option C.
Protista:
This is a kingdom that compromises mostly single-celled organisms (such as: Protazoa)
C. They're carriers of a genetic disorder.
Genetic testing can help screen for variants/mutations in potential parents' DNA. If one or both parents test negative, they will know their child will not inherit the disorder. Likewise, if they both are carriers, there is a chance their child could be affected, which is helpful information in determining whether to have their own children, or how to address their child's possible disorder.
They form into more molecules as they produce more
Liters because liters are larger than milliliters.
