Did Humans Have a Tail?
Human tailbone or coccyx is a vestigial organ and is reminiscent of the tail, which is present for some period... View Article
Human tailbone or coccyx is a vestigial organ and is reminiscent of the tail, which is present for some period... View Article
The two main causes of variation are mutation and genetic recombination in sexual reproduction. Further reading: Adaptive Radiation Microevolution Organic... View Article
Haemophilia is a bleeding disorder, which is caused due to deficiency of blood clotting factors. Haemophilia A is caused due... View Article
Blood clotting factors are named in Roman numerals, e.g. I, II, VIII, IX, etc. Factor IX is also called the... View Article
Haemophilia is an X-linked recessive disorder. Haemophilia is more common in males because they have only one X-chromosome and defect... View Article
If two alleles of a gene are A and a, then p and q represent the frequencies of dominant and... View Article
Inbreeding increases homozygosity. It increases the risk of offsprings with homozygous recessive alleles, which have deleterious effects. Further reading: Molecular... View Article
Factor 9 or IX is a clotting factor, which is involved in blood clotting. Defect in the gene leading to... View Article
Factors that affect Hardy Weinberg equilibrium are gene migration, genetic drift, natural selection, mutation and genetic recombination. These factors change... View Article
Haemophilia is a sex-linked inherited disorder. It is an X-linked recessive disease. Men with haemophilia genes pass it on to... View Article
Haemophilia can be detected before birth by doing prenatal testing such as chorionic villus sampling (CVS) or amniocentesis. Further reading:... View Article
Phenotype frequency is the proportion of individuals showing a particular trait or phenotype in the population. Further reading: Adaptive Radiation... View Article
Allele frequencies of a population can be changed by natural selection, gene flow, genetic drift, mutation and genetic recombination. They... View Article
The two letters in a genotype represent the pair of alleles. The uppercase letter represents the dominant allele and the... View Article
Haemophilia is a genetic disorder, which is caused due to mutation in the gene coding for clotting factors. Haemophilia A... View Article
Mutations may occur due to error at the time of DNA replication or due to external factors such as UV... View Article
Haemophilia is rare in women due to its inheritance pattern. It is an X-linked recessive trait. Females have two copies... View Article
Although 99.9% of the genome is the same in all people, yet every individual has unique DNA, which accounts for... View Article
Phenotype frequency for a particular phenotype is calculated by dividing the number of individuals of the particular phenotype by the... View Article
Humans share around 98.7 percent genome with chimpanzees. Bonobos are also closest to humans and are very similar to chimpanzees.... View Article