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What else can I help you with?
A carrier is a person who has-?
a person who maybe carring the baby
If a male homozygous for the normal gene order and a female homozygous for an inversion mutation had a child the child would have what type or types of chromosomes?
The child would inherit one set of chromosomes from each parent. Since the male is homozygous for the normal gene order, he will pass on a normal chromosome set. The female, being homozygous for the inversion mutation, will pass on chromosomes that carry the inversion. As a result, the child will have one set of normal chromosomes and one set with the inversion mutation, leading to a genotype that is heterozygous for the inversion.
When a child is born chromosomal mutation when did the mutation occur?
During meiosis
When a child is born with a chromosomal mutation when did mutation occur?
during meiosis
Will a baby be born with marfan syndrome if father has it?
There is a 50% chance that the baby will have Marfan. The father might pass on the gene that has the Marfan mutation, or he might pass on the gene that does not. Each child you have together has a 50% chance.
When a child is born with a chromosomal mutation when did the mutation occurs?
during meiosis
Will a mutation in a human skin cell pass on to the persons offspring?
If you are referring to a mutation in individual cells of the skin, then no.
Why do persons having a mutation pass this condition on to their offspring?
Individuals with a mutation can pass it on to their offspring because the mutation is present in their germline cells (sperm or eggs), which are used to create offspring. This means that the genetic mutation is incorporated into the DNA of the offspring, resulting in them inheriting the mutation.
What could be described as a chromosomal mutation?
Chromosomal mutation can have lasting impacts on the person who this happens to. A version of a chromosomal mutation is the mutation that leads to Down's Syndrome.
What happens if a person with mutation reproduce?
If a person with a mutation reproduces, there is a chance that the mutation may be inherited by their offspring. Whether the mutation will be passed on and expressed in future generations depends on the type of mutation and its mode of inheritance. Some mutations are harmful, while others can be neutral or even beneficial.
Is fabry disease contagious?
No. It is genetic and inherited from parent to child It is also X linked witch means that men pass it to daughters and women have a 50% chance of passing the mutation on to any children
Can cytoplasmic mutation be transmitted from parents to their child?
only the hereditary character can be transmitted and it is found in nucleus not in cytoplasm so the cytoplasmic mutation can not be transmitted from parents to their child. hope u get the answer
