A structural chromosomal abnormality is described by which of the following?
Answer
Chromosome breakage with improper repair
Nondisjunction of chromosomes during Meiosis I
Nondisjunction of chromosomes during Meiosis II
Extra chromosomes created and added to genome
Question 2
Question
How many chromosomes could someone with polypoidy have?
Answer
69 chromosomes
47 chromosomes
45 chromosomes
Question 3
Question
You can survive with only one X chromosome.
Answer
True
False
Question 4
Question
Dispermy results in?
Answer
Triploidy
Tetraploidy
Polyploidy
Question 5
Question
The most common pregnancy complication is [blank_start]spontaneous abortions[blank_end].
Answer
spontaneous abortions
Question 6
Question
A baby is born with feet shaped like rockers and clenched hands. The baby had poor prenatal growth. Which of the following describe the condition of the baby?
Answer
Edwards Syndrome, Nondisjunction
Edwards Syndrome, Robertsonian Translocation
Patau Syndrome, Nondisjuction
Patau Syndrome, Robertsonian Translocation
Question 7
Question
All of the following include trisomy. Down Syndrome is a defect in chromosome [blank_start]21[blank_end]. Edwards Syndrome is a defect in chromosome [blank_start]18[blank_end]. Patau is a defect in chromosome [blank_start]13[blank_end].
Answer
13
21
18
22
19
17
15
25
Question 8
Question
Turner Syndrome is a result of nondisjunction of maternal chromosomes.
Answer
True
False
Question 9
Question
The Turner Syndrome genotype is [blank_start]X[blank_end]. The Klinefelter genotype is [blank_start]XXY[blank_end]. The Tripe X Syndrome genotype is [blank_start]XXX[blank_end]. The last sex chromosome disorder involves paternal meiosis II nondisjunction and is called [blank_start]47, XYY[blank_end]
Answer
X
XXY
XXX
47, XYY
Question 10
Question
Which of the following (more than one?) could be caused by maternal nondisjuction?
Answer
Turner Syndrome
Triple X Syndrome
Klinefelter Syndrome
Edwards Syndrome
Question 11
Question
Which of the following would result in a phenotypically normal individual?
Answer
Robertsonian translocation
Deletion
Duplication
Isochromosome
Question 12
Question
Which of the following would describe a male with a balanced reciprocal translocation involving 3q and 17p?
Answer
44 Structurally normal chromosomes
An abnormal phenotype
No increased risk of miscarriage
1 structurally abnormal chromosome
Question 13
Question
A 4 month old female infant is not obtaining normal developmental milestones and has failure to thrive. Chromosome analysis reveals an abnormality; one copy of chromosome 21 has extra genetic material attached to the long arm. The origin of the extra material is not obvious. All other chromosomes appear normal. How would you interpret this finding?
Answer
She has down syndrome
She has a partial trisomy 21
This was inherited from one of her parents who has a balanced abnormal segregation.
The abnormality could be phenotypically mild.
Question 14
Question
A monosomy is worse than a trisomy.
Answer
True
False
Question 15
Question
A baby is born with only one chromosome 15 with the two q arms attached at one centromere. Which of the following most correctly describes the baby's condition.