Answer:
1/8 (12.5%)
Explanation:
An autosomal recessive disease is an inherited disease in which an individual need to receive both defective alleles at the same gene <em>locus</em> to be expressed in the phenotype. In this case, both parents are carriers of the recessive mutant allele associated with the sickle cell anaemia trait, thereby both parents are heterozygous, ie., each parent has one copy of the normal allele 'H' and one copy of the defective mutant allele 'h' associated with this condition. In consequence, their first child has a 1/4 (25%) chance of having sickle-cell anaemia. Moreover, the chance of having a girl is 1/2 and the chance of having a boy is 1/2, thereby the final chance of having a girl sickle cell anaemia individual is 1/4 x 1/2 = 1/8 (12.5%).
- Parental cross for sickle cell anaemia trait = Hh x Hh >>
- F1 = 1/4 HH (normal); 1/2 Hh (normal); 1/4 hh (sickle cell anaemia) >>
- Sex proportion of sickle cell anaemia individuals = 1/8 female sickle cell anaemia individuals + 1/8 male sickle cell anaemia individuals (1/8 + 1/8 = 1/4)
1.) A nucleotide of DNA consists of a sugar, a phosphate, and a nitrogen containing base.
2.) A mutation is a change in the base sequence of a DNA molecule
Hope this helps!
Homeostasis is maintained by negative feedback loops within the organism. In contrast, positive feedback loops push the organism further out of homeostasis, but may be necessary for life to occur. Homeostasis is controlled by the nervous and endocrine systems in mammals.
Satellites, I’m assuming this is what you were looking for as it monitors everything.