Genetics Quiz Questions Flashcards
T/F The genetic information needed for protein synthesis is encoded in the DNA contained in the cell nucleus.
True
T/F Polygenic inheritance can be predicted utilizing the Mendelian laws of genetic transmission.
False- single gene disorders
T/F Messenger RNA carries the instructions for protein synthesis
True
T/F The genotype refers to the recognizable traits, physical or biochemical, associated with a specific phenotype.
False- The PHENOTYPE refers to the recognizable traits, physical or biochemical, associated with a specific GENOTYPE
T/F The Punnett square can be utilized to describe possible combinations that can occur with transmission of single-gene dominant and recessive traits.
True
T/F Ribosomal is the type of RNA that functions to deliver the activated form of amino acids to protein molecules in the ribosomes.
False- tRNA
T/F Autosomal recessive disorders are manifested even if only one member of the gene pair is affected.
False- Autosomal DOMINANT disorders
T/F A teratogenic agent is an environmental agent that produces abnormalities only during the first 4 weeks of embryonic or fetal development
False - 15-50 days
T/F Down syndrome, Turner syndrome and Klinefelter syndrome are all examples of chromosomal disorders that occur from an alteration in chromosome number.
True
T/F Sex-linked disorders almost always are associated with the X chromosome and are predominantly recessive.
True
Which of the following statements about CF is correct?
- CF is an autosomal dominant trait
- CF results from a mutation in the CFTR gene, which normally encodes a chloride ion channel
- the most common mutation associated with CF is a single nucleotide polymorphism (point mutation) in the CFTR gene
- Normally individuals with a mutation in the CFTR have a normal sweat test
A person with cystic fibrosis may be at risk of bleeding due to:
- Excessive fat digestion
- Decreased vitamin K absorption
- Compromised chloride ion transport
- Increased secretions throughout the gut
A person with CF may have decrased fertility
T/F
True
Two parents with the trait for sickle cell disease (so they are heterozygotes) have a child. What is the risk of that child having sickle cell disease?
- 0%
- 25%
- 50%
- 100%
Many of the s/s of SCD (hyperbillirubinema, decreased hematocrit, enlarged liver and spleen) are due to excessive hemolysis experienced by individuals with SCD
True