Answer:
a. A hypothesis that does not generate a testable prediction is not useful.
Explanation:
In the scientific method, we generate a hypothesis to explain a phenomenon. After this, it is necessary to create a method to test the hypothesis and make predictions. Moving forward, we test this methodology, generating results and reject or not reject the hypothesis. If the hypothesis can't be tested, the scientific method can't be applied.
Answer:
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Explanation:
The new coronavirus causes severe inflammation in your lungs. It damages the cells and tissue that line the air sacs in your lungs. These sacs are where the oxygen you breathe is processed and delivered to your blood.
Plant Kingdom to species is 24,000 or more species are broken up into three groups/division: Mosses, Liverworts, and Hornworts.
The secondary structure consists of local packing of polypeptide chain into α-helices and β-sheets due to hydrogen bonds between peptide bond – central carbon backbone.
Red-green color blindness is due to a mutant gene in the X chromosome. An XX female with normal color vision and an XY male with normal color vision have a child with karyotype XXY who is color blind. The likely explanation is that the:_--------.
father was heterozygous for the color-blindness mutation.
mother was heterozygous for the color-blind mutation.
father had CNV of the color-blind mutation.
mother had CNV of the color-blind mutation.
None of the other answer options is correct.
Answer:
mother was heterozygous for the color-blind mutation.
Explanation:
Colorblindness is a recessive disorder. This means that it is expressed only in homozygous genotypes. The responsible gene is present on the X chromosomes. A colorblind female would have the genotype X^cX^c where c is the recessive allele of the gene present on the X chromosome responsible for color blindness. A female with genotype X^cX would have normal visible but would serve as a carrier.
Both the female and the male have normal genotype. Since they had a colorblind child, it means that the female was a heterozygous carrier for the trait and imparted the responsible allele to the child. The male can not serve as a carrier for X linked recessive disorder since they have only one copy of the X chromosome. Therefore, the female was a heterozygous carrier.
