Answer:google
Explanation: i would take eveything you put n here ad go one google and search this up
Answer:
The correct answer is ''The scientific study of heredity''
Explanation:
Genetics is a branch of biology that studies how hereditary characters are transmitted from generation to generation and the diversity that exists among living beings. Inheritance is the physical and biological characteristics that we share with our family and that can determine our appearance and our biological characteristics, that is, our phenotype (eye color, skin type, etc.) as well as our internal characteristics. All of this is largely derived from our genetic components, that is, our genotype.
A single-celled organism floats freely and lives independently. Its single cell is able to carry out all the processes of life without any help from other cells.
• A biofilm is a thin layer of bacteria that sticks to a surface. Cells in a biofilm are all alike, but they may play different roles, such as taking in nutrients or making the "glue" that sticks the biofilm to the surface. The sticky plaque that forms on teeth is a biofilm of bacterial cells.
• Some single-celled organisms, such as algae, live in colonies. A colony is an organized structure composed of many cells, like the Volvox sphere in Figure 3.21. Volvox are algae that live in colonies of hundreds of cells. All of the cells in the colony live and work cooperatively. For example, they can coordinate the movement of their flagella, allowing them to swim together through the water as though they were part of a single organism.
A multicellular organism consists of many cells and has different types of cells that are specialized for various functions. All the cells work together and depend on each other to carry out the life processes of the organism. Individual cells are unable to survive on their own.
i got this off of quizlet so i hope this helps you. Also this isnt plagarizim bc i gave you where i got it from.
Answer:
"Between the sugar and the phosphate of adjacent nucleotides" this statement correctly identifies the location of the hydrogen bonds in DNA.
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.
