they derive from a common ancestor. a homology is a "structural correspondence".
Homology among proteins and DNA is often concluded on the basis of sequence similarity, especially in bioinformatics. For example, in general, if two or more genes have highly similar DNA sequences, it is likely that they are homologous. But sequence similarity may also arise without common ancestry: short sequences may be similar by chance, and sequences may be similar because both were selected to bind to a particular protein, such as a transcription factor. Such sequences are similar but not homologous.
Homologous chromosomes are identified by two main characteristics viz, size and position of the centromere.
Homologous chromosomes always have the same size. According to the position of the centromere, they may be acrocentric, metacentric, sub-metacentric and telocentric.
Homologues are chromosome pairs of the same length, centromere position, and staining pattern with genes for the same characteristics at corresponding locations. One homologous chromosome is inherited from the organism's mother, the other from the organism's father during sexual reproduction. The crossing over, or synapse, occurs during meiosis, which is the process of exchanging genetic material for recessive or dominant genes between the two homologous chromosomes for better genetic combinations in the formation of gamets.
Homologous chromosomes look alike & they have the same length & centromere position.
Chromosomes normally occur as homologous pairs in a diploid cell. These refers to matching pairs of chromosomes which are found in the cell.
They are called homologous chromosomes (but can also be referred to as homologues or homologs).
A human gamete does not have any pairs of homologous chromosomes. A single human gamete contains 23 chromosomes, or a half set. None of these chromosomes are homologous with each other.
Human cells have 23 homologous pairs. They also must go through meiosis before that. Females have 2 X chromosomes, while Males have an X and a Y chromosome. That's why the males cells decide the gender of the child.
there are 23 pairs of matching chromosomes 46 chromosomes altogether.
Homologous pairs of chromosomes are not normally found in a zygote.
Chromosomes normally occur as homologous pairs in a diploid cell. These refers to matching pairs of chromosomes which are found in the cell.
It has pairs of matching chromosomes.
They are called homologous chromosomes (but can also be referred to as homologues or homologs).
A human gamete does not have any pairs of homologous chromosomes. A single human gamete contains 23 chromosomes, or a half set. None of these chromosomes are homologous with each other.
chromosome pairs
Human cells have 23 homologous pairs. They also must go through meiosis before that. Females have 2 X chromosomes, while Males have an X and a Y chromosome. That's why the males cells decide the gender of the child.
Homologous chromosomes
there are 23 pairs of matching chromosomes 46 chromosomes altogether.
homologous chromosomes are chromosome pairs that code for the same features such as eye color or hair color, one chromosome of the pair comes from your mom and one from your dad so no they are not identical
Nothing
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