I don't know what your choices are, but I did the questions for you.
R=D/2, R=12, R=radius,
SA= 4 times 3.14 12 times 12, so,
SA=1809.557368, if you round it to two decimal places, it'll be,
1809.56, so the answer is 1809.56in. squared.
Answer:
Step-by-step explanation:
hello :
note :
Use the point-slope formula.
y - y_1 = m(x - x_1) when : x_1= -3 y_1= -2 m= 1/2(parallel means same slope)
an equation in the point-slope form is : y +2 = 1/2(x+3)
Mandy Increases her books by 2 per month.
Bill increases his books by 4 per month.
Month Mandy Bill
May 18 4
June 20 8
July 22 12
August 24 16
Sept 26 20
Oct 28 24
Nov 30 28
Dec 32 32
At the end of December they will have read the same amount of books.
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)
