it must be autosomal as it is in chromosome 1 which both genders have.
No, a gene is either autosomal or sex-linked, but never both.
No it is autosomal
G6PD deficiency is caused by one copy of a defective G6PD gene in males or two copies of a defective G6PD gene in females. Hemolytic anemic attacks can be caused by oxidants, infection, and or by eating fava beans.
The Spina Bifida birth defect is autosomal.
Not really. Autosomal refers to the fact that a characteristic is controlled at a single genetic locus. Sex linked refers to a gene locus on the sex chromosomes For example. Hemophilia is a sex linked characteristic because the genetic locus for the disease is located on the X sex chromosome. It is also autosomal recessive.
No, it is autosomal, with the likely gene mutation located on the short arm of chromosome 6.
This is sex linked and is inherited through the parents.
When the gene is dominant and the traits are autosomal.
gene that is not strong
It's an autosomal dominant disease. Source: http://en.wikipedia.org/wiki/Achondroplasia
Cystic fibrosis (CF) is an autosomal recessive disorder, not an X-linked disorder. It means that both copies of the gene responsible for CF need to be mutated in order to develop the disorder. Incomplete dominance refers to a genetic trait where the heterozygous condition results in an intermediate phenotype, which is not the case for CF.
It's sex-linked recessive because the defect is on the X-chromosome. It's more common in male because of this fact. In order for a female to have it, she'd have to have defective genes on both of her X-chromosomes.yes, colour blindness is passed through the mother's gene