Question
Which of the following does not result in variations among siblings?
Independent assortment of genes
Crossing over
Linkage
Mutation
Independent assortment of genes
Crossing over
Linkage
Mutation
Hint:
The genes are closely related when the linkage occurs
The correct answer is: Linkage
- The proximity of genes or other DNA sequences to each other on the same chromosome.
- The closer two genes or sequences are on the chromosome, the more likely they are to be inherited together.
Related Questions to study
Identify the wrong statement about meiosis
Identify the wrong statement about meiosis
A diploid cell with a diploid number of 24 chromosomes undergoes meiosis. How many chromosomes are present in each daughter cell after division?
A diploid cell with a diploid number of 24 chromosomes undergoes meiosis. How many chromosomes are present in each daughter cell after division?
What type of cell division occurs in cells of testes and ovaries?
What type of cell division occurs in cells of testes and ovaries?
Meiosis results in _____.
Meiosis results in _____.
Meiosis I is reductional division, and meiosis II is equational division because of
Meiosis I is reductional division, and meiosis II is equational division because of
Meiotic division takes place in
Meiotic division takes place in
Meiosis is of evolutionary significance as it produces
Meiosis is of evolutionary significance as it produces
What is the importance of crossover?
What is the importance of crossover?
Which of the following structures are formed by two homologous chromosomes pair during crossing over?
Which of the following structures are formed by two homologous chromosomes pair during crossing over?
In prophase I of meiosis I __________ occurs.
In prophase I of meiosis I __________ occurs.
What structures exchange genetic material during crossing over?
What structures exchange genetic material during crossing over?
Hemophilia disease is produced in the male by how many gene/s?
- Genetic disorders can be chromosomal, multifactorial and monogenic
- Hemophilia is a blood disorder that delays blood clotting or hemostasis
- Blood clotting is a result of cascade of reactions done by clotting factors (1 to 12)
- Absence of clotting factor VIII or IX causes hemophilia
- Gene (F8 or F9) responsible for hemophilia is present in X chromosome
Hemophilia disease is produced in the male by how many gene/s?
- Genetic disorders can be chromosomal, multifactorial and monogenic
- Hemophilia is a blood disorder that delays blood clotting or hemostasis
- Blood clotting is a result of cascade of reactions done by clotting factors (1 to 12)
- Absence of clotting factor VIII or IX causes hemophilia
- Gene (F8 or F9) responsible for hemophilia is present in X chromosome
How do genetic disorders happen?
- Genetic disorder is due to alteration in gene sequence
- The gene sequence change can occur in a cell irrespective of type of cell division a cell undergoes
- Mutation can occur at any point of cell division
- Trisomy can be attributed as a result of meiosis
How do genetic disorders happen?
- Genetic disorder is due to alteration in gene sequence
- The gene sequence change can occur in a cell irrespective of type of cell division a cell undergoes
- Mutation can occur at any point of cell division
- Trisomy can be attributed as a result of meiosis
In Down’s syndrome of a male child, the sex chromosome is
- Down syndrome is a genetic disorder
- It is a trisomy condition having extra copy of chromosome 21
- The individual affected will have disability associated with nervous system
- Sex chromosome remains unaffected irrespective of the disorder
In Down’s syndrome of a male child, the sex chromosome is
- Down syndrome is a genetic disorder
- It is a trisomy condition having extra copy of chromosome 21
- The individual affected will have disability associated with nervous system
- Sex chromosome remains unaffected irrespective of the disorder
Which one is a hereditary disease?
- Pleiotropy is a condition where a single gene is responsible for control of multiple unrelated traits of an individual
- Individuals with phenylketonuria lack the ability to process phenylalanine to tyrosine due to absence of an enzyme, This results is decreased metabolism.
- Leprosy is caused by Mycobaterium leprae
- Cataract and general blindness are caused due to environmental interferences
Which one is a hereditary disease?
- Pleiotropy is a condition where a single gene is responsible for control of multiple unrelated traits of an individual
- Individuals with phenylketonuria lack the ability to process phenylalanine to tyrosine due to absence of an enzyme, This results is decreased metabolism.
- Leprosy is caused by Mycobaterium leprae
- Cataract and general blindness are caused due to environmental interferences