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∙ 6y agoHomozygous
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∙ 12y agoAnonymous
dominant allele
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ihih
A method of illustrating what chromosomes are present.
A given gene is present on exactly two chromosomes in a somatic cell.
In humans, 46 chromosomes are present when meiosis begins. The four daughter cells that result from meiosis have 23 chromosomes.
The structure present in the nuclear region of a living cell that bears genes is the nucleus. Within the nucleus, genes are located on long strands of DNA called chromosomes. These chromosomes contain the genetic information necessary for the cell's functioning and development.
If both members of a pair of chromosomes are present in the cell, the condition of the chromosomes is said to be diploid. Diploid cells have two sets of chromosomes, one set derived from each parent.
23 chromosomes are present in spermatids
XX chromosomes.
chromosomes are present in the nucleus of zygote.
A method of illustrating what chromosomes are present.
In humans, 46 chromosomes are present when meiosis begins. The four daughter cells that result from meiosis have 23 chromosomes.
Chromosomes are seen in the nucleus of the eukaryotic cells.
A given gene is present on exactly two chromosomes in a somatic cell.
In humans, 46 chromosomes are present when meiosis begins. The four daughter cells that result from meiosis have 23 chromosomes.
Genes for traits are contained within the chromosomes, which are found in the cell's nucleus. Each gene is a segment of DNA that encodes a specific trait or characteristic. Genes are passed down from parents to offspring during reproduction.
The structure present in the nuclear region of a living cell that bears genes is the nucleus. Within the nucleus, genes are located on long strands of DNA called chromosomes. These chromosomes contain the genetic information necessary for the cell's functioning and development.
yes chromosomes are present when cell divide
One example of a disorder associated with an error in the number of chromosomes present is Down syndrome. This disorder is caused by the presence of an extra copy of chromosome 21, leading to characteristic physical features and often intellectual disability.