Answer:
The father
Explanation:
Turner syndrome is a monosony condition resulting from the fusion of normal gamete with a gamete lacking a chromosome. The resulting zygote lacks in one chromosome. In human, Turner syndrome is deleterious in males and only occur in female.
Color blindness is a X-linked recessive trait. A male with XY chromosome will need just a copy of the allele while a normal XX female will need 2 copies (one from each parent). A X-0 female (Turner syndrome) only need a copy of the recessive allele.
Since both parents have normal vision, it means that the father was not affected for the disease and the affected X chromosome must have been from the carrier mother. It thus means that the missing X chromosome is the fault of the father.
<em>Therefore non-disjunction of the XY chromosome must have happened in the father leading to inability to contribute a X chromosome to the daughter.</em>
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Ionic is the answer. Hope this helps!
Answer:
Its DNA
Explanation:
Each RNA nucleotide consists of three parts: a sugar, a phosphate group, and a nitrogen-containing base. The four RNA bases are adenine, uracil, guanine, and cytosine—often referred to as A, U, G, and C. RNA shares three bases in common with DNA: adenine, guanine, and cytosine. Instead of uracil, DNA contains thymine.
DNA is made up of molecules called nucleotides. Each nucleotide contains a phosphate group, a sugar group and a nitrogen base. The four types of nitrogen bases are adenine (A), thymine (T), guanine (G) and cytosine (C). The order of these bases is what determines DNA's instructions, or genetic code.
Answer:
I think it may be C Transformation...I might be wrong though....I'm sorry if I am
Explanation: