Answer:
Since sickle cell disease is a disorder with an autosomal dominant inheritance pattern, and in light of the lack of data, it could be said that the only way for Pat and Tracy to have a child with sickle cell disease is for both of them to be healthy carriers of the gene, with a 25% probability.
Explanation:
Considering that both Pat and Tracy each have a sibling with a sickle cell trait and that both they and their parents are healthy, it must be assumed that some of their parents are healthy carriers:
- Pat and Tracy do not have sickle cell trait. In this case, there is no chance that they will have a child with sickle cell disease.
- Either Pat or Tracy has the trait, but the other does not. It is possible that at least one of their children is a healthy carrier.
- If both Tracy and Pat have sickle cell trait, the chances of having a child with sickle cell disease are:
Alelles R r
R RR Rr
r Rr rr
RR: healthy (25%).
Rr: healthy carrier (50%).
rr: sickle cell disease (25%).
<em>If Pat and Tracy are healthy carriers of the gene that determines sickle cell disease, the chance of having a child with the disease is 25%</em>.
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Autosomal recesive inheritance brainly.com/question/10605612
Answer:
The hypha is the building block of a fungus. On the other hand, mycelium refers to the collection of hyphae in a fungus' body. 2. Hyphae are often described as strands, threads, or filaments because of their appearance.
Answer:
Variation, in biology, any difference between cells, individual organisms, or groups of organisms of any species caused either by genetic differences (genotypic variation) or by the effect of environmental factors on the expression of the genetic potentials (phenotypic variation). Variation may be shown in physical appearance, metabolism, fertility, mode of reproduction, behaviour, learning and mental ability, and other obvious or measurable characters.
chromosomes or by differences in the genes carried by the chromosomes. Eye colour, body form, and disease resistance are genotypic variations. Individuals with multiple sets of chromosomes are called polyploid; many common plants have two or more times the normal number of chromosomes, and new species may arise by this type of variation. A variation cannot be identified as genotypic by observation of the organism; breeding experiments must be performed under controlled environmental conditions to determine whether or not the alteration is inheritable.
Genotypic variations are caused by differences in number or structure of Environmentally caused variations may result from one factor or the combined effects of several factors, such as climate, food supply, and actions of other organisms. Phenotypic variations also include stages in an organism’s life cycle and seasonal variations in an individual. These variations do not involve any hereditary alteration and in general are not transmitted to future generations; consequently, they are not significant in the process of evolution.
Explanation:
Brainliest please?