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XA Xa
Al Leuschke
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∙ 6y agoXA Xa
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What is true of a woman with the genotype?
She is a carrier of hemophilia but does not have the condition
Which phenotype is displayed in an individual with the genotype?
A man who does not have hemophilia
Hemophilia is a sex linked recessive disorder Mary does not have the disease but both of her brothers do Neither of her parents have the disease What are Marys parents genotypes indicates pr?
Mary's father is normal and has a normal genotype XY while her mother is the carrier of hemophilia and has one X of her genotype infected i.e. she is X*X.
If you know a woman has hemophilia what can you infer about her parents genetype?
Her father has to have hemophilia as well, and the mother is a carrier or also has hemophilia. So if we pretend that the hemophilia gene is "x", you need to have "xx" to have hemophilia. The father must have the genotype "Yx" and the mother has the have "Xx" or "xx".
If an individual marries a person with the same genotype as another. what is the chance that one of their children will be afflicted with hemophilia?
the chance would be 50%
What whoud be the result of a normal women having a child with a hemophilia men?
All Girls will be carriers of Hemophilia and all Males will be unaffected (they won't have Hemophilia).
In human the allele for hemophilia h is recessive. which phenotype is displayed in an individual with the genotype?
Genes that come together with different alleles are called _____.
In humans the alleles for hemophilia h is recessive. Which phenotype is displayed in an individual with the genotype XhY?
Genes that come together with different alleles are called _____.
What color is a person with AAbb genotype?
if a man were non- hemophiliac and he marries a woman whois homozygus for nan-hemophilia,give the possible genotypes of the children
How an organism looks as a result of its genotype is known as its?
Phenotype
Royal hemophilia is the result of what inheritance?
Hemophilia is broken into three subcategories; Hemophilia A, Hemophilia B, and Hemophilia C. These subcategories designate a person as having a deficiency of one of three specific clotting proteins. Hemophilia A is the deficiency of the protein called Clotting Factor VIII. Hemophilia B is the deficiency of Clotting Factor IX. Hemophilia C is the deficiency of Clotting Factor XI. "Royal" hemophilia is simply a reference to Hemophilia B and is therefore a result of a deficiency in the Clotting Factor IX protein. It is sometimes called the royal disease because it has been known to have been passed through some royal families throughout history.
Is hemophilia a hereditary disease or acquired from microorganisms?
Hemophilia is not acquired from microorganisms. Hemophilia is typically a genetic disorder that can either be inherited or result from a random mutation. In rare cases non genetic forms (that can not be inherited or passed on) of hemophilia can be acquired due to liver impairment, and certain medications.
