Answer:
Hemophilia is a x-linked recessive inherited bleeding disorder. in this disease blood does not clot properly due to the decreased level of blood clotting factor VIII (8) or factor IX (9).
In x-linked recessive condition, the disease is transmitted from father (affected male) to his daughter and mother (affected female) to her son and skip of generation getting affected is also occurs.
- there will be 50% chance of her (S.R.) each son to be affected with hemophilia.
Explanation:
Hemophilia is caused due to mutation of one gene which is responsible for the making of proteins of blood coagulation factor viii or ix. the affected person bleeds continuously from any injury and that can cause serious issues.
here,
grandfather of s.r is affected (xₐy) and grandmother is normal (xx) will produce
↓
s.r's mother who is a carrier (xₐx) [as xₐy and xx will produce 100% carrier xₐx daughter]
↓
s.r's mother is a carrier (xₐx) but her father is normal (xy) will produce,
↓
s.r who has 50% chance of being carrier (xₐx) and 50% chance of being normal (xx) [as she is the only child] and she has a normal (xy) partner, they will give,
↓
- if s.r is a carrier (xₐx) then one of her son will be affected (xₐy) [as xₐx and xy =xₐy]
- if s.r is normal (xx) then her son will be normal (xy) [as xx and xy will give xy]
here,<u> 50% chance of her son to be affected with hemophilia</u> [as S.R of being affected is more considerable].
Answer:
harvesting of light energy and its transfer to the core
Explanation:
basically, the antennas are ablet o pick up light which is then transferred as energy.
Answer:
Atom
Explanation:
An atom is the most simple and basic form of matter which cannot be broken down any further.
Answer:
Thymus vulgaris (Thyme)
This plant is generally known as thyme. The characterization of thyme oil by GC and GC-MS methods indicated that thymol (40.5%), p-cymene (23.6%), carvacrol (3.2%), linalool (5.4%), β-caryphyllene (2.6%), and terpinen-4-ol (0.7%) are present in thyme EO.
Explanation:
mark me branliest
Answer:
Explanation:
Since Mark's wife was a carrier, it means that she is heterozygous for the trait. And after Mark got tested, they decided to have children due to no increased risk if they do have children, it means the condition is not an autosomal dominant condition but a recessive condition because if the condition is dominant, only one copy of the affected allele is needed to increase risk.
Thus, with a no increased risk, it means Mark is normal i.e. carries no copy of the recessive allele.
