Are u using a punnet square for children or for genotypes
A group of cells that work together to perform a common function
Answer:
Hemophilia is a sex-linked recessive disorder in which a person's blood do not clots and he can bleed to death even after minor injuries because blood will keep running due to a small cut.
It is a recessive trait which means that even if one normal gene is present along with Hemophiliac gene, the person will not have the disease and he will be the carrier.
Question: What will be their children’s possible phenotypes?
If a woman who is a carrier for hemophilia marries a hemophiliac man, their genotypes can be denotes as :
Here H, indicate normal gene and small h indicate defected (hemophilia) gene.
Parents: XHXh X XhY
Offspring: XHXh : XHY: XhXh: XhY
Phenotype of offspring:
XHXh: The child will be daughter and normal (25 % chances)
XHY: The child will be son and normal (25 % chances)
XhXh: The child will be girl and Hemophiliac (25 % chances)
XhY: The child will be son and Hemophiliac (25 % chances)
Hope it helps!
Answer:
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Explanation:
Step 1: Glycolysis. In glycolysis, glucose—a six-carbon sugar—undergoes a series of chemical transformations. In the end, it gets converted into two molecules of pyruvate, a three-carbon organic molecule. In these reactions, ATP is made, and \text{NAD}^+NAD + N, A, D, superscript is converted to {NADH}NADHN, A, D, H.
Step 2:Pyruvate oxidation. Each pyruvate from glycolysis goes into the mitochondrial matrix—the innermost compartment of mitochondria. There, it’s converted into a two-carbon molecule bound to Co-enzyme A, known as acetyl CoA. Carbon dioxide is released and NADH is generated.
Step 3:Citric acid cycle. The acetyl CoA made in the last step combines with a four carbon molecule and goes through a cycle or reaction, ultimately regenerating the four carbon starting molecule.