Plz .what sex is the person who has the karyotype described in steps 3-4? how do you know?
2.in what ways are the mutations described in steps 5-6 and 7-8 different from those described in steps 9-10 and 11-12?
3.in steps 11-12, you saw that cystic fibrosis is caused when specific sections of both copies of chromosome 8 are deleted. on the basis of this information, do you think cystic fibrosis is a dominant or recessive trait?
4.do all mutations result in negative effects?