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a Chromosome
X
genetic defects are responsible for disorders can be on any chromosome wether it is and autosome or a sex chromosome.
The difference between a chromosome and a DNA molecule is that a chromosome is a single DNA molecule associated with proteins and a DNA molecule is a long thin molecule that stores genetic information.
two loci on human chromosomes 1 and 14 respectively that are linked to migraine headaches. The locus on chromosome 1q23 has been linked to familial hemiplegic migraine type 2, while the locus on chromosome 14q21 is associated with migraine without aura
Chromosome 21.
a Chromosome
chromosome.
No, it is autosomal, with the likely gene mutation located on the short arm of chromosome 6.
A distinctive, painful skin rash, called dermatitis herpetiformis, may be the first sign of celiac disease. Approximately 10% of patients with celiac disease have this rash
The most common condition associated with a deletion of the end of chromosome 5 is: cri-du-chat syndrome.
Periventricular heterotopia is associated with abnormalities of the filamin1 gene on the X chromosome.
chromosome
X
The symptoms of celiac disease can be different from person to person and can mimic many other illnesses. It can cause irritability, cramps, mouth sores, rash or stomach pain.
Genetic defects can be associated with autosome and chromosome abnormalities.
Yes. Usually if a someone is diagnosed with celiac, they will have other family members with the disease. Anoother associated allergy to celiac is lactose-intolerance. (allergy to milk).Yes, celiac disease is a hereditary disease. A doctor can determine if you suffer from it.