In a dominant cross, the chance of the dominant phenotype showing up in one of the offspring is 3/4, since the dominant genes are being shown here.
The statement which is true about the inheritance of hemophilia is that it is a recessive trait on the X chromosome. Thus, the correct option for this question is C.
<h3>What is Hemophilia?</h3>
Hemophilia may be defined as an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery.
Hemophilia is significantly caused by the lack of clotting factor VIII or IX in the blood. In most cases, hemophilia is passed down through families (inherited). Most of the time, it is passed to male children. Several women in the family were carriers of the allele for the disorder, only men ended up actually expressing the disorder.
Therefore, the statement which is true about the inheritance of hemophilia is that it is a recessive trait on the X chromosome. Thus, the correct option for this question is C.
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Answer:
You need to use the scientific method and <u>knowledge of the environment and earth systems</u> in order to work as an environmental scientist.
Explanation:
An environmental scientist works based on the fact that it has the knowledge of the environment and he is aware of the interaction between the environment and other components associated with it.
An environmental scientist study about the effect of environment on plants and animals as well as earth systems to protect, understand and develop research methods.
Answer:
It is habitat and then niche
Explanation:
I just answered it
Answer:
1) The alleles for homozygous brown hair will be BB.
2) The alleles for heterozygous brown hair will be Bb
3) Let's make a punnet square to check for the outcomes:
B b
B BB Bb
B BB Bb
4) The results from the punnet square depict that the phenotype of all the children produced will be brown hair.
5) The punnet square depicts that there will be a 50% probability of the child to carry the heterozygous genome (Bb) and there is also 50% probability for the child to carry homozygous dominant genome (BB).