A pedigree shows the genotypes of the family members
in autosomal recessive disorders, the diseased genes are inherited from the parents. For the person to get the disease both diseased genes should be there in the genotype as its a recessive disorder.
the dominant gene - H
recessive gene - h
for a person to get a disease, genotype should be hh, as its autosomal recessive. If the person is normal he/ she could have the genotype HH or could be Hh and thats called a carrier.
the offspring will receive one gene from the mother and one from the father
the answer to your question is the amount of time and the effect it has on each material as well as the fact that the nitrogen cannot change it is an unchangeable variable whereas everything else the time, the substance of the subject, the possible formation of nodules can change without changing the identity of the experiment itself otherwise, you have a dependent variable. I hope this helps :-)
Answer:
Explanation:
As you probably already know, all of the cells in your body started from a single cell. That single cell then divided many, many times to turn into the 50 trillion or so cells that make up you. Almost all of the cells in your body share the same DNA as was found in that first cell
The components that make up the genetic code are common to all organisms! Same NUCLEOTIDES, same BACKBONE same BASE-PAIRS, same HYDROGEN BONDS! The instructions for making proteins (and traits) are in the sequence of nucleotides! These are the GENES that hold our similarities or differences
C. is deactivated in a strongly acidic solution