Japanese
I'm pretty sure that wasnt one of the options
The "autosomal dominant" method of inheritance. if your question as Marfan syndrome is the result of inheriting a single allele. Individuals with Marfan syndrome are tall and long-limbed, and have both cardiovascular and eye defects. The inheritance of Marfan syndrome is an example of ______. then the answer is pleiotropy
The inheritance of Marfan syndrome is an example of an autosomal dominant genetic disorder. This means that a person only needs to inherit one copy of the mutated gene from one parent in order to develop the condition.
Apert syndrome is typically caused by a sporadic mutation in the FGFR2 gene and is not inherited in a simple dominant or recessive manner. It is considered an autosomal dominant condition, with most cases arising from new mutations.
Pleiotropy.
Some autosomal disorders in humans that are controlled by dominant alleles include Huntington's disease, Marfan syndrome, and neurofibromatosis type 1. These disorders are expressed when an individual inherits a single copy of the mutated gene from one parent.
The "autosomal dominant" method of inheritance. if your question as Marfan syndrome is the result of inheriting a single allele. Individuals with Marfan syndrome are tall and long-limbed, and have both cardiovascular and eye defects. The inheritance of Marfan syndrome is an example of ______. then the answer is pleiotropy
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
Marfan syndrome is an inherited disorder that is typically passed down from one generation to the next through an autosomal dominant pattern of inheritance. This means that if one parent carries the Marfan syndrome gene, there is a 50% chance that they will pass it on to each of their children. In some cases, Marfan syndrome may also occur as a result of a spontaneous genetic mutation.
The inheritance of Marfan syndrome is an example of an autosomal dominant genetic disorder. This means that a person only needs to inherit one copy of the mutated gene from one parent in order to develop the condition.
Apert syndrome is typically caused by a sporadic mutation in the FGFR2 gene and is not inherited in a simple dominant or recessive manner. It is considered an autosomal dominant condition, with most cases arising from new mutations.
Pleiotropy.
100% of the offspring will display the dominant trait because the homozygous dominant parent can only pass on the dominant allele. The offspring will inherit one dominant allele from the dominant parent and one recessive allele from the recessive parent, resulting in a heterozygous genotype expressing the dominant trait.
Edward's syndrome is not technically recessive or dominant, because it is not caused by a single gene. Rather it happens due to a trisomy of chromosome 18 (or just of a part of said chromosome). Parent's may be healthy and still have offspring with the syndrome not because its recessive, but because the trisomy arises during meiosis of the gametes. Whatever happens to the gametes affects only the offspring not the carrier parent.
Some autosomal disorders in humans that are controlled by dominant alleles include Huntington's disease, Marfan syndrome, and neurofibromatosis type 1. These disorders are expressed when an individual inherits a single copy of the mutated gene from one parent.
About 1 in 5,000 people have Marfan syndrome, including men and women of all races and ethnic groups. About 3 out of 4 people with Marfan syndrome inherit it, meaning they get the genetic mutation from a parent who has it. But some people with Marfan syndrome are the first in their family to have it; when this happens it is called a spontaneous mutation. There is a 50 percent chance that a person with Marfan syndrome will pass along the genetic mutation each time they have a child.
Yes you get your eye color from your parent. The parent that carries one dominant gene and one recessive gene for a specific eye color and the other parent carries two recessive genes for a different eye color, you will get the eye color of the parent who carries the dominant and recessive gene. In other words, the dominant gene trumps the recessive gene. In another scenario, if both parents carry two recessive genes for a specific eye color, then you will inherit the recessive gene of that color.
It is a genetic disorder and if one parent has it, there is a 50?50 chance that the child will have it.