Some scientists say:
-The insulin dependent DDM1, Diabtese mellitus is on chromosome 6
-Type 1 Diabetes was found on chromosome 1q42, and possibly 11
-Type 2 Diabetes on Chromosomes 12 and/or 20
Not exactly. Galactosemia is a genetic mutation that can happen on a chromosome. (Chromosome 9 to be exact.)
It affects the 50th chromosome by mutation
It's a defect of the 9th chromosome
two copies of every gene located on the X chromosome.
The gene for free ears is located on chromosome 22. If the ears are attached, this is due to gene "Z".
This means that the gene is physically located on that particular chromosome.
The farthest apart two genes are located on a chromosome the less likely they are to be inherited together. If two genes are on the same chromosome and rarely assort independently the genes are probably located close to each other.
Galactosemia is a genetic disorder which is caused by a lack of the GALT enzyme. This is essential in breaking down the milk sugar galactose.
The health condition galactosemia occurs when the body has a deficiency in processing glucose. The condition mostly affects infants and can be life threatening if not treated.
Galactosemia... the word "lactose" in this word should have given you a thoughtless answer.
A metacentric chromosome is one in which the centromere is located in the center of the chromosome.
It's located on the X chromosome.
chromosome 4
Galactosemia II is caused by defects in both copies of the gene that codes for an enzyme called galactokinase (GALK). The frequency of occurrence of galactosemia II is about one in 100,000-155,000 births.
The gene that causes cystic fibrosis is located on chromosome 7, which is an autosome, not a sex chromosome.
chromosome 7 according to the internet
The Factor X gene is said to be located on the X chromosome. Females have two X chromosomes, whereas males only have one. The other chromosome they have is a Y chromosome.
two copies of every gene located on the X chromosome.
everywhere
Genes are located within every chromosome.