विषम-युग्मकज इसके अंग्रेजी अर्थ का उदाहरण

Although it is an autosomal recessive disorder, heterozygotes may still manifest much attenuated symptoms.

Instead of decreased mRNA levels, a mutant transcript produces truncated β chains, which in turn leads to a clinical phenotype in the heterozygote.

Individuals with a single mutation in one of the spectrin genes are usually asymptomatic, but those who are homozygotes or are compound heterozygotes (i.

Furthermore, heterozygotes, those who have one normal allele and one coding for the disease, also show relatively shortened telomeres.

Studies also reveal that a transferrin saturation (serum iron concentration ÷ total iron binding capacity) over 60 percent in men and over 50 percent in women identified the presence of an abnormality in iron metabolism (Hereditary hemochromatosis, heterozygotes and homozygotes) with approximately 95 percent accuracy.

Most heterozygotes, with few exceptions, do not have a bleeding diathesis.