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>.
Learn more:
Autosomal recesive inheritance brainly.com/question/10605612
Answer:
the answer is D
Explanation:
The prefix bi indicates that the muscle has two origins
The biceps femoris muscle of the leg derives its name from having two heads of origin, long and short
Cellular respiration is needed for atp to be made. it needs sunlight, glucose and oxygen. i’m pretty sure the main answer would just be glucose and oxygen though.
The right answer is metaphase II.
The process is performed in two nuclear and cytoplasmic divisions, called first and second meiotic division or simply meiosis I and meiosis II. Both include prophase, metaphase, anaphase, and telophase. First division prophase is long and consists of 5 stages: leptotene, zygotene, pachytene, diplotene, and diakinesis. It is at this point that genetic recombination takes place at the level of chiasmus.
During meiosis I, the members of each homologous pair of chromosomes are paired during prophase, forming bivalents. During this phase, a protein structure, called synaptonemal complex form, allows recombination between homologous chromosomes. Subsequently, a large condensation of the bivalent chromosomes occurs and go to the metaphase plate during the first metaphase, resulting in the migration of n chromosomes to each of the poles during the first anaphase. This reduction division is responsible for maintaining the number of chromosomes characteristic of each species.
In meiosis II, as in mitosis, the sister chromatids comprising each chromosome are separated and distributed between the nuclei of the daughter cells. Between these two successive steps, there is no DNA replication. The maturation of the daughter cells will result in the gametes.
