Red-green color blindness is an X-linked recessive disorder that is passed through generations and can be traced by using a pedigree. A pedigree is shown. Sam, Bella, Joshua, and Tim have filled-in shapes. Lisa and Monica have half-filled shapes.

Which individuals in the pedigree are identified and labeled carriers for red-green color blindness?
Lisa and Monica
Sam, Tim, Bella, and Joshua
Ben, Jenny, Mike, Carol, Katie, and Chris
Ben and Lisa

Lisa and monica

Explanation:

just took the test :))

answer: tributaries flow into rivers.

wetland is a biome that develops when the water gets accumulated in a land exhibiting a huge depression. these form either seasonally or permanently. the water in the wetland comes from rivers, lakes, ocean, flood, rain or other sources. the wetlands includes mangroves, marshes and peatland.

tributaries flow into the rivers develops a wetland because such water will get deposited in the depression and will restrict the original flow of tributary water. hence, water with low drainage current combines with the river water.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.