Nz=4326380 people divided by the area 103736mlz=42 people per square miles.
avs=21905140 people divided by 296909mlz=7 people mlz
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.
I think it may be this but not quite sure
Lipids are primarily hydrophobic in nature, but there are a large variety of lipids such as fatty acids, mono-, di-, and triglycerides, for example (check wikipedia for more examples).
<span>Proteins are polymers of amino acids. </span>
<span>Nucleic acids are polymers of nucleotides.</span>
Answer:
The correct answer is: B. If he inherited a mutation which made him more susceptible to lung cancer, it may have been present in some of the gametes he produced and passed to his children.
Explanation:
- The inheritance of genes from the parents to the offspring is mediated by the germinal cells or sex cells or gametes of the parents.
- The genetic material present in the somatic cells of the parents are not transmitted to the offspring.
- In the given case, the man who develops lung cancer generates some tobacco smoke induced mutations in some of the cells of his lungs.
- The cells of the lungs are type up of somatic cells. Hence, any mutations in the genome of these cells will never be transmitted to the offspring.
- Therefore, the children of the man will never become prone to develop lung cancer due to development of mutations in the lung cells of the man.
- However, if the man has inherited any mutation from his parents which can increase the risk of development of lung cancer, then these mutations will be present in his germinal cells and also in some of his gametes.
- Now, if a child is born due to the fusion of the the maternal gamete with one of these mutated paternal gametes, there is an increased chance of developing lung cancer in the child, irrespective of the fact whether he is a smoker or a non-smoker.
