Answer:
Chromosomal Mutation
Explanation:
The development and function of an organism is in large part controlled by genes. Mutations can lead to changes in the structure of an encoded protein or to a decrease or complete loss in its expression. Because a change in the DNA sequence affects all copies of the encoded protein, mutations can be particularly damaging to a cell or organism. In contrast, any alterations in the sequences of RNA or protein molecules that occur during their synthesis are less serious because many copies of each RNA and protein are synthesized.
Geneticists often distinguish between the genotype and phenotype of an organism. Strictly speaking, the entire set of genes carried by an individual is its genotype, whereas the function and physical appearance of an individual is referred to as its phenotype. However, the two terms commonly are used in a more restricted sense: genotype usually denotes whether an individual carries mutations in a single gene (or a small number of genes), and phenotype denotes the physical and functional consequences of that genotype.
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Answer:
ok this is point less but whatever you want
Turner syndrome occurs when the individual inherits only one (female) X chromosome.
<h3>What is Chromosome?</h3>
This is referred to a thread like structure which contains DNA and protein components.
An individual inheriting only one female X chromosome means that the child will have turner syndrome which is characterized by short height, heart defects etc.
The complete question is:
Which condition occurs when the individual inherits only one (female) X chromosome?
Read more about Turner syndrome here brainly.com/question/953084
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