Deletion
cystic fibrosis
Yes they can if you want to have AIDS!
sickle cell anaemia, thalassaemia
all of these (study island answer) or for regular info... the deletion of a gene caused by an error in chromosomal crossover, the duplication of a gene caused by an error in chromosomal crossover, a transposition that replicates and inserts new copies of itself within an organism's genome
1. (1) Produced by an abnormality in, or a mutation of the genetic code in a single gene; (2) Caused by several abnormal genes (Producing so-called polygenic diseases); or (3) Caused by the abnormal presence or absence of an entire chromosome or by alteration in the structure of chromosomes.
Wolf-Hirschhorn syndrome is primarily caused by a deletion of a portion of chromosome 4, specifically at the 4p16.3 region. This chromosomal mutation is classified as a deletion mutation, where a segment of the chromosome is missing, leading to the loss of genetic material. The syndrome is characterized by developmental delays, distinctive facial features, and other congenital anomalies.
Huntington's disease is caused by a gene mutation, specifically in the HTT gene on chromosome 4.
Usher syndrome is a relatively rare genetic disorder caused by a mutation. The gene is not carried on one of the sex chromosomes (X or Y).
cancer
No, galactosemia is not a type of chromosomal mutation. It is a genetic disorder caused by mutations in specific genes that are involved in the metabolism of galactose, primarily the GALT gene. These mutations lead to an inability to properly process galactose, resulting in toxic accumulation. Chromosomal mutations involve changes in the structure or number of chromosomes, which is different from the single-gene mutations seen in galactosemia.
Neither. It is an extra #21 chromosome.
Yes, it is caused by a mutation in the gene for the protein CFTR.
a) mutation b) allele c) gene d) replicator
nodules
This type of mutation is called a translocation mutation. It involves the movement of a segment of DNA from one chromosome to another non-homologous chromosome, leading to potential genetic changes and abnormalities.
There are many thousands of different mutations.
No, Marfan syndrome is not a chromosomal abnormality. It is a genetic disorder caused by a mutation in the fibrillin-1 (FBN1) gene, which affects the body's connective tissue. This gene is located on chromosome 15.