Human Genetics: Inheritance of Single-Gene Differences

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18 Questions

What is a major limitation of using humans as research subjects in genetics?

Their long life cycle

Which of the following is NOT a method used to study human genetics?

Randomized controlled trials

What can be detected through karyotyping?

Numerical and structural abnormalities

What type of inheritance pattern is characterized by the trait never skipping a generation?

Autosomal Dominant

What is the primary method used in human genetics?

Pedigree Analysis

What type of marriage would produce offspring that are also affected by the trait?

Marriage between two affected individuals

What is the characteristic of metacentric chromosomes in terms of centromere position?

centromeres in the middle of the chromosome

Which group of human chromosomes has a medium size and acrocentric centromere location?

Group D

What is the chromosomal composition of Turner's Syndrome?

22II+ X0

Which type of chromosomal aberration is characterized by 22II+ I21+ XX or XY?

Down's Syndrome

What is the centromere location of chromosomes in Group G?

acrocentric

Which of the following chromosomal aberrations is characterized by 22II+XXX?

Metafemale

What is the key characteristic of Autosomal Dominant inheritance?

No skipping of generations is observed

What is the most likely explanation for the occurrence of cystic fibrosis in a population?

Matings between heterozygotes

What is the pattern of inheritance observed in Sex-linked Recessive traits?

Affected families with unaffected husbands transmit the trait to sons only

What is the key difference between Autosomal Dominant and Autosomal Recessive inheritance?

The presence of skipping of generations

What is the probability of having a child with an autosomal recessive disorder if both parents are carriers of the gene?

1 in 4

What is the reason for increased consanguinity between parents in Autosomal Recessive Disorders?

Because most matings are with relatives

This quiz covers the reasons why humans are unsuitable research subjects and the methods used to study human genetics, including pedigree analysis and karyotyping.

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