Step-by-step explanation:
The standard form for a line is Ax+By=C
First, we need to find the slope, or change in y over change in x. For the first one, this is
, which is impossible to find as we cannot divide by 0, meaning that this is constant horizontally -- in this case, x=2. Thus, we have 1*x+0*y=2.
For the second one, we can find the slope by getting
. We can then take the point (3,0) (it can be any point on the line) and get our equation to be y-0 = (-2/3) (x-3). Converting this to standard form, we can expand this to get
y= (-2/3)*x +2
(-2/3)*x+1*y = 2
Step-by-step explanation:
can you please add details to your question
-8 = -7x-1
bring -1 to the other side as we are isolating for x so it will be
-7 = -7x then divide -7 from each side
-7/-7 = (-7/-7)x
1 = x
Answer is f(1)= -8
Answer:
Pedigrees of autosomal recessive traits will have equal frequencies of affected males and females, whereas pedigrees X-linked recessive traits will show that most of the affected individuals are male.
Step-by-step explanation:
If the trait is dominant, one of the parents must have the trait. Dominant traits will not skip a generation. If the trait is recessive, neither parent is required to have the trait since they can be heterozygous.A pedigree is a chart which shows the inheritance of a trait over several generations. From studying a pedigree, scientists can determine if a trait is sex-linked or autosoma If an individual has that trait, their symbol on the pedigree will be shaded in. If they have no widow's peak, their symbol will not be shaded in because having no widow's peak is recessive. Certain traits like colorblindness are located on the X or Y chromosome and are called sex-linked Several basic modes of inheritance exist for single-gene disorders: autosomal dominant, autosomal recessive, X-linked dominant, and X-linked recessive. However, not all genetic conditions will follow these patterns, and other rare forms of inheritance such as mitochondrial inheritance exist Autosomal recessive patterns manifest by skipping generations as the affected are usually children of unaffected carriers. It is also common to see affected individuals with unaffected offspring. ... The most common situation of an autosomal recessive disease occurs when the parents are each carrier or heterozygous (Dd)
Answer:
C
Step-by-step explanation:
2z + xy
Put z as 3, x as 4, and y as 6.
2(3) + (4)(6)
Multiply the terms.
6 + 24
Add both terms.
= 30
