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during meiosis

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Drew Tremblay

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3y ago

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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 the mutation occurs?

during meiosis


When a child is born with a chromosomol mutation when did the mutation occur?

A chromosomal mutation can occur either during the formation of the egg or sperm, or after fertilization when the zygote is forming. This means the mutation could have occurred in the parent's gametes, or during cell division in the early stages of embryo development.


If child is born with trisomy when did the mutation occur?

during meiosis


If a child is born with down syndrome when did the mutation occur?

During meiosis


How many toes is a human baby born with?

A normal human baby is born with 10 toes, 5 on each foot. Occasionally a genetic mutation will occur and baby will be born with more or less toes.


How many toes is a human baby born?

A normal human baby is born with 10 toes, 5 on each foot. Occasionally a genetic mutation will occur and baby will be born with more or less toes.


How many toes is a human baby born-with?

A normal human baby is born with 10 toes, 5 on each foot. Occasionally a genetic mutation will occur and baby will be born with more or less toes.


How many toes is baby human born with?

A normal human baby is born with 10 toes, 5 on each foot. Occasionally a genetic mutation will occur and baby will be born with more or less toes.


What happens when zygotes have serious chromosomal problems?

Most zygotes with serious chromosomal problems are born with severe mental and physical disabilities; many die before being born or shortly thereafter.


What Type Of Mutation is Polydactyly?

Polydactyly is a type of genetic mutation that results in individuals being born with extra fingers or toes. It is usually an inherited trait, although it can also occur spontaneously. Polydactyly is considered a rare condition.


How do you get Down syndrome?

You do not "get" Down's syndrome. You are born with it. It is a chromosomal condition of the 21st chromosome.