The correct answer is option B. Genotype AA, phenotype-Unaffected.
The cystic fibrosis is a condition caused by the inheritance of the two recessive allele, It is an autosomal recessive disease.
In the given case, the parents are carriers, and the carriers are always heterozygotes. Hence, the phenotype of the both parent should be Aa. A possible cross of the parents is shown in the figure below.
In case, the progeny have a single dominant trait, the child would not be affected, but will be a carrier and can pass the disease to offspring. In case, the child inherit both the dominant allele (homozygous dominant) from the parents, then he/she would be unaffected. In case, the phenotype of the child is homozygous recessive then it would be affected.
The given blank can be filled with liver.
The huge surface area of the small intestine helps in absorption of nutrients. The water-soluble nutrients and small fats enter the bloodstream directly. The inner surface of the small intestine comprises hundreds of folds of compositions known as villi. Within the villi, there are numerous microscopic projections known as microvilli.
The microvilli substantially enhance the surface area of the small intestine that upsurges the rate of absorption of nutrients. Upon entering the bloodstream the water-soluble nutrients are directed towards the liver prior to being transported to the cells.
The statistical study of all populations is called demography
The limit of ecosystems to give advantages to people, that is to give biological community administrations, gets from natural cycles of water, nitrogen, carbon, and phosphorus. These procedures have now and again been altogether altered by human movement. Changes have been quicker in the second 50% of the twentieth century than at some other time in recorded mankind's history.
