The answer is D. This means that is you have a determined amount of force (in newtons) being applied on an object of known mass (in kilograms), then to determine the acceleration of the object, divide the force by the mass (or multiplying the force with the inverse of the mass of the object). This behavior of objects is stipulated in Newtons/ second law. Increasing the force increases the acceleration while increasing the mass decreases the acceleration of the object. Acceleration is a vector quantity meaning it has magnitude and direction.
The answer to this question is phase. These three properties, amplitude, frequency and phase are basic properties of waves. Frequency refers to the number of cycles per second, amplitude refers to the strength, and phase is the position of the wave on the time axis.
Answer:
Sickle cell disease in an autosomal recessive inherited disease which is caused by the mutation in the HBB (hemoglobin-β gene) gene present on the chromosome no. 11. In sickle cell, the red blood cells become sickle shape due to the abnormal shape of hemoglobin present in it.
These sickle cells are known to form a blockage in the blood vessels thereby causing damage to the vital organs. Human spleen constantly destroys sickle cells because they get trapped in it which causes a disease called sickle cell anemia.
Sickle cell anemia is normally the problem in genetic disease which is inherited from the parents to children. When both the DNA strand has a mutation in their HBB gene then only this disease will affect the individual.
Root hair cells absorb minerals and water from the soil.
The water absorbed by the root hair cells passes through the plant in xylem tubes, to then reach the leaves. The energy from the sun is then used to convert water(H2O) into hydrogen (H) and oxygen(O2).
I hope this helps
1.) Achodroplasia is a autosomal dominant disorder, the suspected case suggested that inorder for the parents to produce and offspring with achondroplasia. One parents must have a single mutant gene of achodroplasia to be inherited by his offspring. for this case, It is suggested that the offspring might have developed its own mutant gene as it only affect 1 in 25,000 birth. There is changes of genes during early development.
2.) The mother said that they don't have that history of disorder. again, it's autosomal dominant disorder. one parents must have that kind of disorder so their child can also inherit it. Thus, no of the childs parents is a carrier.
