āĻ āĻ¨ā§āĻ¸āĻ¨ā§āĻ§āĻžāĻ¨ āĻāĻ°ā§āĻ¨
āĻ āĻāĻŋāĻ§āĻžāĻ¨ā§āĻ° āĻāĻžāĻˇāĻž āĻ¨āĻŋāĻ°ā§āĻŦāĻžāĻāĻ¨ āĻāĻ°ā§āĻ¨
āĻāĻĒāĻ¨āĻžāĻ° āĻāĻžāĻˇāĻž āĻ¨āĻŋāĻ°ā§āĻŦāĻžāĻāĻ¨ āĻāĻ°ā§āĻ¨
autosome
/ËÉËtÉĘsËÉĘm/
Autosome
01
āĻ āĻā§āĻ¸ā§āĻŽ, āĻ˛āĻŋāĻā§āĻ āĻā§āĻ°ā§āĻŽā§āĻ¸ā§āĻŽ āĻ¨āĻ¯āĻŧ
any chromosome that is not involved in determining sex, present in pairs in both males and females, and carrying most of an individual's genetic information
āĻāĻĻāĻžāĻšāĻ°āĻŖ
Genetic disorders such as cystic fibrosis are linked to mutations in autosomes.
āĻ¸āĻŋāĻ¸ā§āĻāĻŋāĻ āĻĢāĻžāĻāĻŦā§āĻ°ā§āĻ¸āĻŋāĻ¸ā§āĻ° āĻŽāĻ¤ā§ āĻāĻŋāĻ¨āĻāĻ¤ āĻŦā§āĻ¯āĻžāĻ§āĻŋāĻā§āĻ˛āĻŋ āĻ
āĻā§āĻ¸ā§āĻŽ-āĻ āĻŽāĻŋāĻāĻā§āĻļāĻ¨ā§āĻ° āĻ¸āĻžāĻĨā§ āĻ¯ā§āĻā§āĻ¤āĨ¤
āĻļāĻŦā§āĻĻāĻ¤āĻžāĻ¤ā§āĻ¤ā§āĻŦāĻŋāĻ āĻāĻžāĻ
autosomal
autosome
āĻ¨āĻŋāĻāĻāĻŦāĻ°ā§āĻ¤ā§ āĻļāĻŦā§āĻĻ
