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There are several causes of Anglemann syndrome. None of them are inherited as a dominant recessive or co-dominant characteristics. The most common cause (68% of cases) is a deletion of the q12 region of the maternally derived chromosome 15.
trait
relating to or denoting heritable characteristics controlled by genes that are expressed in offspring only when inherited from both parents, i.e., when not masked by a dominant characteristic inherited from one parent.
Kleinfelters is a chromosomal "trisomy" of the sex chromosomes. It is not inherited in a recessive or dominant manner.
The inheritance of a dominant and a recessive allele results in a blending of traits to produce intermediate characteristics.
There are several causes of Anglemann syndrome. None of them are inherited as a dominant recessive or co-dominant characteristics. The most common cause (68% of cases) is a deletion of the q12 region of the maternally derived chromosome 15.
glaucoma is inherited in an autosomal dominantpattern.which is dominant.
When two recessive genes are inherited, and the portion of recessive inheritance is 51% or greater in favor of the recessive trait.
trait
relating to or denoting heritable characteristics controlled by genes that are expressed in offspring only when inherited from both parents, i.e., when not masked by a dominant characteristic inherited from one parent.
It is a sex-linked recessive trait inherited from the mother.
Kleinfelters is a chromosomal "trisomy" of the sex chromosomes. It is not inherited in a recessive or dominant manner.
Recessive gene is one which is supressed and do not show their characteristics and dominant gene is one which show their characteristics for example if a father has brown hair and mother has black hairs and if their son has black hair then in this case gene which has characteristics of black is dominant and the other which has characteristics of brown colour is recessive
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The inheritance of a dominant and a recessive allele results in a blending of traits to produce intermediate characteristics.
it is rarely inherited, and is often spontaneous. but when inherited, it is considered autosomal dominant condition and is usually passed down from someone with the condition to all of their offspring
Similarty: They both come from inherited parents.