Answer: B (Color blindness)
Explanation:
Typical red-green color blindness in human patients is caused by mutations on genes located in the X chromosome. These mutations act in a recessive manner. Since females have two X chromosomes, the presence of a mutation in a single one of them does not normally result in color blindness. Males, in contrast, have a single X chromosome and therefore the presence of a mutation is likely to cause the disease.
About the other options: Down‘s syndrome is a numerical chromosomal anomaly, not related to sex. Human blood type is a codominant trait. Finally, tail length in dogs is a polygenic trait not amenable to classic Mendelian analysis.
Answer:
D
Explanation:
i think tell me if in wrong don't give me any hate
barinist pls thx
I believe it's lactic acid and energy.
a) ribosomes on the rough endoplasmic reticulum
mRNA (created by DNA) leaves the nucleus through the nucleic pores, and from there will enter a nearby ribosome since the rough endoplasmic reticulum is surrounding the nucleus. It is there that polypeptides are made and transported in vesicles to the Golgi apparatus because they cannot touch the cytoplasm when still incomplete. Hope this helped.
