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प्रश्न
Complete the following sentence with appropriate word:
The dissimilar pairs of genes present in an individual are known as _______________.
उत्तर
The dissimilar pairs of genes present in an individual are known as Heterozygous.
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संबंधित प्रश्न
The phenotypic ratio of incomplete dominance is ______.
A cross used to verify the unknown genotype of the F1 hybrid is a ______.
Explain the Term Variation.
Name the following:
The genetic composition of an organism.
Give Technical Term:
Differences occurring within offsprings of the same progeny.
Give Technical Term:
Cell organelle directly involved in genetics.
Mention, if the following statement is True or False. If false rewrite the wrong statement in its correct form:
DNA has a double-helical structure.
Mention, if the following statement is True or False. If false rewrite the wrong statement in its correct form:
Genes are responsible for genetic characters.
Mention, if the following statement is True or False. If false rewrite the wrong statement in its correct form:
Mutation can be brought about artificially.
Multiple Choice Question
When an individual has both the genes of a contrasting character, it is said to be:
Multiple choice question.
A cross between an individual with an unknown genotype for a trait with recessive plant for that trait is _______.
The word chromosome was coined by
Give any two points of difference between homozygous and heterozygous.
A recessive factor is altered by the presence of a dominant factor.
In a dihybrid cross with contrasting characters, the number of different genotypes obtained in F2 generation are ______.
The appearance of new combinations in the F2 generation of a dihybrid cross proves the law of ______.
A normal visioned woman whose father is colourblind married a normal visioned man. What are the probabilities of her sons or daughters to be colourblind? Explain with the help of Punnett square.
During a dihybrid cross with contrasting characters in the F2 generation, parental genotypes will appear in ______.
Name any two genetic diseases in humans.