The Hardy-Weinberg principle is used to characterize the distribution of the different genotype frequencies in a population which are not evolving. In the Hardy-Weinberg equation,
the frequency of the homozygous dominant genotype is denoted by 
;
the frequency of the homozygous recessive genotype is denoted by 
;
the frequency of the heterozygous genotype is denoted by 2pq;
the frequency of the recessive allele is denoted by q;
the frequency of the dominant allele is denoted by p.
A because it’s dna fragments
In my opinion, I think that coal is the most important mineral of all. It keeps us warm during winter and it helps train transport food and other goods that we need.
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Chargaff's rules state: adenine is complimentary to thymine and cytosine is complimentary to guanine. For this question, in order for polymerization of the growing complementary strand, guanine must bind with cytosine.
<span>Answer: B.C</span>
1. The main aim of the Human Genome Project was to determine the DNA Sequence of every human gene.
2. Variation in skin colour is an example of polygenic inheritance
This Human Karyotype is unusual because it has an extra chromosome at chromosome 21.
Klinefelters syndrome is shown in the second figure
Explanation:
1. The Human Genome Project's main goal was to sequence all the 30,000 genes and 3 million base pairs in their makeup for the early detection of diseases, gene therapy and molecular level studies.
2. Human skin colour is determined by the pigment melanin. The Dominant allele is responsible for dark colours as it produces more melanin. The melanocortin 1 receptor (MC1R) gene and Tyrosinase enzyme codes for the human skin colour. Polygenic inheritance are the traits which are controlled by one or more genes.
<u>figures:</u>
<u>The extra chro</u>mosome at the 21st chromosome pairs is called trisomy 21 or Down's Syndrome. It is due to the abnormal cell division/meiosis resulting in an extra X chromosome. This leads to thechanges the in physical development of the individual.
Klinefelter's Syndrome: There are 47 chromosomes and 2 or more X chromosomes in this syndrome of males. The resulting male suffering from Klinefelter would be sterile and have poorly developed testicles.
