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What happens when chromosome 13 and 14 switched parts of their chromsomes?
Wiki User
∙ 14y ago
I think you mean translocation between chromosomes 13 and 14.
Transfiguration is a type of magic taught at Hogwarts School of Wizardry or, on a far more profound level, can also refer to the episode in the life of Christ where he appears before the disciples radiating light.
Wiki User
∙ 11y ago
Wiki User
∙ 14y agoLook up "Robertson Translocation".
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The difference between deletion duplication inversion and translocation?
Deletions are a loss of all or part of a chromosome. Duplications produce extra copies of parts of a chromosome. Inversions reverse the direction of parts of a chromosome. Translocations occur when part of one chromosome breaks off and attaches to another.
What parts of a chromosome specify the amino acid sequence of a protein?
the sequence of bases
When a chromosome is made of two identical parts are called?
Well in eukaryotic cells each chromosome has a telomere on each end (to prevent it from unraveling), but I'm not 100% certain that these telomeres are identical although they contain very long repetitions of the same nucleotides. But in bacteria the chromosome is ring shaped and is all genes (there are no noncoding sequences, e.g. centromeres, telomeres, introns, pseudogenes, transposons) so there are no identical parts.
What are the parts of the DNA code on chromosomes?
This answer will discuss the parts of a eukaryotic chromosome. Chromosomes consist of highly condensed DNA also called chromatin. The chromatin is organized into two arms: the shorter p arm and the longer q arm. Each chromosome contains a highly condensed region that separates the arms of the chromosome. This condensed region is called the centromere. The terminal ends of the chromosome are called telomere.
What is bigger chromosomes nucleus genes?
The chromosomes are lot bigger in size than the genes. The genetic material in packed into genes and then genes are expressed or located on the chromosomes. The chromosome and the genes are very important structures in the study of the genetic and must be carefully studied.
What happens if you are born without chromosome 16?
Children born without parts of chromosome 16 can have problems with growth disorders and anomalies with the head, face and internal organs.
Gene A occurs on chromosome 5 gene B on chromosome 21 Therefore these two parts of a chromosome cannot be what?
alleles
What is a list of the 3 parts of a chromosome?
Telomere - The ends of the chromosome. Centromere - The primary constriction of the chromosome. Chromatid - A single molecule of DNA. The centromere also divides the chromosome into a short arm (p) and a long arm (q).
The difference between deletion duplication inversion and translocation?
Deletions are a loss of all or part of a chromosome. Duplications produce extra copies of parts of a chromosome. Inversions reverse the direction of parts of a chromosome. Translocations occur when part of one chromosome breaks off and attaches to another.
What is the point of a chromosome where two parts meet?
The Centromere
The structure that holds the 2 parts of the chromosome together?
Centromere.
What parts of a cell contains hereditary materials?
the mitochondria
What are the parts of a chromosome that control inherited traits?
The parts of a chromosome that control inherited traits is referred to as genes. There are many types of inherited traits, some visible while the others are invisible,
Suppose your looking through a microscope and you see an exchange of chromosome segments between chromosome pair 7 and chromosome pair 15?
An exchange of chromosome segments is called a translocation. In genetics, it refers to a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes.
What is the name for each of the two identical parts of a double chromosome?
chromatid
Body parts starting with the letter x?
There is the xiphoid process (a small piece of cartilage at the base of your sternum)XX chromosome...orXY chromosome:)
What are the differences between translocation and inversion mutations?
Translocation is when nonhomologous chromosomes exchange segments, like when chromosome 1 exchanges parts with chromosome 5. Inversion is when broken segments of the chromosome is inserted backwards.
