They include: trans-location, deletion, duplication and inversion. A chromosome mutation is an unpredictable change that occurs in a chromosome.
a bunch of stuff acxtually 4 major mutations to look at these go to Google and type in your question. if this does not work for you then sucks for you
Mutations differ and change according to many factors: 1- Site of occurrence: -Genetic mutations -Chromosomal mutations 2- The inheritance: -Somatic mutations -Gamete mutations 3- The origin: -Spontaneous (natural) mutations -Induced mutations 4- The harmful OR useful effects: -Undesirable mutations -Desirable mutations
No, they were actually on 4 chromosomes. Here is the quoted text: "Although it is true that Mendel could not have found more than 7 traits that could have been unlinked by virtue of the fact that the genes determining those traits reside on separate chromosomes it turns out that the traits he studied were confined to only 4 chromosomes; chromosome 1 for traits 2 and 3, chromosome 4 for traits 4, 6, and 7, chromosome 5 for trait 5, and chromosome 7 for trait 1."
four
From smallest to largest: DNA (where DNA = short sequences of nucleotides) gene chromosome nucleus sperm cell
Mutations in the alpha-L-iduronidase (IDUA) gene located on chromosome 4 cause the MPS I disorders (Hurler, Hurler-Scheie, and Scheie syndromes
Chromosome 4
A gene mutation is a permanent change in the DNA sequence that makes up a gene. Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome. A chromosomal mutation is a mutation involving a long segment of DNA, it is a any change in the structure or arrangement of the chromosomes. These mutations can involve deletions, insertions, or inversions of sections of DNA. In some cases, deleted sections may attach to other chromosomes, disrupting both the chromosomes that loses the DNA and the one that gains it.It is also referred to as a chromosomal rearrangement The differences between Gene mutation and Chromosome mutation are ; 1- Chromosome mutations involve changes in the structure of a chromosome OR the loss or gain of a chromosome while Gene mutations involve a change in the nucleotide -base sequence of a gene on a DNA molecule. 2- Chromosomal mutations are changes in the structure or the numbers of chromosomes (a gain or loss). Gene mutations involve changes in the nucleotide sequence of the DNA molecule. 3-A gene mutation is a permanent change in the DNA sequence that makes up a gene. Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome while a chromosomal mutation is a mutation involving a long segment of DNA, it is a any change in the structure or arrangement of the chromosomes. These mutations can involve deletions, insertions, or inversions of sections of DNA. In some cases, deleted sections may attach to other chromosomes, disrupting both the chromosomes that loses the DNA and the one that gains it.It is also referred to as a chromosomal rearrangement 4-gene mutation is just a substitute in any old random nucleotide for any old random nucleotide chromosome mutation is missing of chromosome or +1 chromosome (down's syndrome).
No, Chromosome 4.
chromosome 4
in a homologous chromosome there are two chromosomes ( a chromosome and a sister chromosome)
Since the traits for hemophilia are carried on the X chromosome and not the Y, it is more probable for females to have a chromosome with the mutation. Since the mutation is considered recessive and males only have one X chromosome, they are more likely to portray the phenotype for hemophilia than their female counterparts.
autosomal dna, X chromosome, Y chromosome,and mitochondrial
The gene codes for a protein called huntingtin found on the short arm of chromosome 4.
The cast of Chromosome 4 - 2014 includes: Malachi Brown Thea McCartan as Katharine
a bunch of stuff acxtually 4 major mutations to look at these go to Google and type in your question. if this does not work for you then sucks for you
Mutations differ and change according to many factors: 1- Site of occurrence: -Genetic mutations -Chromosomal mutations 2- The inheritance: -Somatic mutations -Gamete mutations 3- The origin: -Spontaneous (natural) mutations -Induced mutations 4- The harmful OR useful effects: -Undesirable mutations -Desirable mutations