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.
Current estimations are that one in five Americans will develop skin cancer in their lifetime. It is estimated that approximately 9,500 people in the U.S. are diagnosed with skin cancer every day. Which adds up to over 3.3 million persons each year.
Hope this helps! :)
Answer:
As my study programme is concerned with the field of biotechnology, I hope that by the end of the proposed study programme, I will be able to gain knowledge about the molecular tools and the concepts and trends in genome editing. I shall be able to perform techniques such as PCR, gel electrophoresis, cell culturing easily. I would be able to grasp better knowledge in the fields of plant biotechnology, animal biotechnology, Industrial biotechnology and marine biotechnology.
Answer:no
Explanation:
Because you could be blind
