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Hemophilia is a genetic disorder that causes a protein required for normal blood clotting to be missing. In a cross with a mother who carries the allele for hemophilia and a father who has normal blood clotting what would be the phenotypes of the offspring?
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Asked 7/26/2016 10:49:57 AM
Updated 7/26/2016 11:10:52 AM
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Flagged by Janet17 [7/26/2016 11:04:23 AM]
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User: Hemophilia is a genetic disorder that causes a protein required for normal blood clotting to be missing. In a cross with a mother who carries the allele for hemophilia and a father who has normal blood clotting what would be the phenotypes of the offspring?

Weegy: Stage 1: The blood vessels is damaged and the bleeding starts. Stage 2: The blood vessels constrict to slow the flow of blood to the injured area. Stage 3: Platelets stick to, and spread on, the walls of damaged blood vessels. [ [ This is called platelet adhesion. These spreading platelets release substances that activate other nearby platelets which clump at the site of injury to form a platelet plug. This called platelet aggregation. ] ]
ajspicer|Points 10|

Question
Asked 7/26/2016 10:49:57 AM
Updated 7/26/2016 11:10:52 AM
1 Answer/Comment
This conversation has been flagged as incorrect.
Flagged by Janet17 [7/26/2016 11:04:23 AM]
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In a cross with a mother who carries the allele for hemophilia and a father who has normal blood clotting, the phenotypes of the offspring would be: one female normal, one male normal, one female carrier, one male with hemophilia.
Added 7/26/2016 11:10:52 AM
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