Many inherited disorders in humans are controlled by a single gene. Achondroplasia is a form of dwarfism. About one out of 25,000 people has achondroplasia. The homozygous dominant genotype causes death of the embryo, and therefore only heterozygotes, individuals with a single copy of the defective allele, have this disorder. This also mean that a person with achondroplasia has a 50% chance of passing the condition on to any children. Achondroplasia is a recessive allele.
yes, dwarfism is a mutation because dwarfism is a permanent gene or chromosome change in the organism.
yes.it is it is y linked to the father and/or themother. it is caused by themutationof the cromosone fort
Yes, it is caused by a mutation in the gene for the protein CFTR.
Yes dwarfism can be considered genetic disorder, however not always.
See link:
http://en.wikipedia.org/wiki/Dwarfism#Classification
No, there are many different types of dwarfism each with a different cause.
Yes. Dwarfism is a genetic disorder.
yes it it
Is there a particular chromosome on which thalassemia is located
They are located on one chromosome.
The only difference in the chromosome is the presence of the allele that results in an individual with acondroplastic dwarfism. The chromosome affects the structure of the organism, the allele affects the growth plates of the long bones resulting shortened limbs.
A metacentric chromosome is one in which the centromere is located in the center of the chromosome.
DNA or genens these are the segments of the chromosome.
Is there a particular chromosome on which thalassemia is located
69 haha just kidding
This means that the gene is physically located on that particular chromosome.
They are located on one chromosome.
it is a mutation of the gene FRG3 in chromosome 4
The only difference in the chromosome is the presence of the allele that results in an individual with acondroplastic dwarfism. The chromosome affects the structure of the organism, the allele affects the growth plates of the long bones resulting shortened limbs.
A metacentric chromosome is one in which the centromere is located in the center of the chromosome.
DNA or genens these are the segments of the chromosome.
It's located on the X chromosome.
chromosome 4
Some studies have isolated defects for the production of pituitary hormones to the short arm (the "p" end) of chromosome 3 at a specific location of 3p11. Other studies have found changes on the short arm of chromosome 7.
The gene that causes cystic fibrosis is located on chromosome 7, which is an autosome, not a sex chromosome.