1. is a process of gaining and testing knowledge & must be proven through experimentation. 2.or non-science claims to be scientific but does not use experimentation. Cryptozoology is an example of this.

Explanation:

Science is the study of nature and behavior of everything around us. It is the knowledge on the physical or material world obtained through observation and experimentation.

Pseudoscience incorporates convictions, speculations, or practices that have been or are viewed as logical, however have no premise in scientific fact. This could mean they were invalidated experimentally, can't be tried logically, or need proof to help them. The term commonly has a negative implication. At the point when utilized, somebody's intimating the theme did not depend on logical discoveries and is, in this manner, ailing in truth.

equal distribution i think.

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.