Euploid - Samenvattingen, Aantekeningen en Examens
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Genetic Syndromes |89 questions| with correct answers
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Chromosomal Defects CORRECT ANSWER Euploid-Normal chromosome number 
Aneuploidy-Abnormal chromosome number 
Monosomy-Turner 
Trisomy-Trisomy 13, 18, 21, Klinefelters XXY 
 
Trisomy 21 
*Down Syndrome CORRECT ANSWER MR 
Hypotonia 
Endocardial cushion defects 
Duodenal atresia 
Brushfield spots 
Simian crease 
Early alzheimer dz 
Polycythemia 
Hirschsprungs disease 
Increased ALL risk 
Sandle gap toes 
3-4% due to Robertsonian translocation, the rest have extra chromosome 
 
Risk factor for Trisom...
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Study Stack for Midterm SCI 225 || All Answers Are Correct 100%.
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Tay-Sachs disease correct answers A disease that results in accumlation of lipids, in the nerve cells of the brain. 
 
What causes metaplasia in humans? correct answers cell injury from noxious (poisonous) stimuli 
 
Algor Mortis correct answers The cooling of the body after death 
 
Dysplasia is characterized by correct answers abnormal changes in cell secretions 
 
Clastogens correct answers agents tht cause chromosomal breakage 
 
What is tatooing and stippling? correct answers Gunshot wounds...
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MMSC490 Quiz 3 (Actual quiz with 100% verified answers)
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Eggs and sperm are 
tetraploid. 
haploid. 
euploid. 
diploid correct answers haploid Animal cells and most cells of higher plants are 
haploid. 
tetraploid. 
euploid. 
diploid. correct answers diploid 
 
 
 
Our fundamental knowledge about mutation, genetic linkage, and the relationships between genes and chromosomes was acquired largely from experiments on the 
plant Maize. 
pea plant. 
fruit fly Drosophila. 
bacterium Pneumococcus. correct answers fruit fly Drosophila. 
 
George Beadle and Edw...
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Pathophysiology Exam Paper 1 Questions with Correct Answers
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An ordered photographic display of a set of chromosomes from a single cell is a(n): 
A) metaphase spread. 
B) autosomal spread. 
C) karyotype. 
D) anaphase spread. - Answer -c 
 
An error in which homologous chromosomes fail to separate during meiosis is termed: 
A) aneuploidy. 
B) nondisjunction. 
C) polyploidy. 
D) anaplasia. - Answer -b 
 
A somatic cell that does not contain a multiple of 23 chromosomes is called: 
A) an aneuploid cell. 
B) a euploid cell. 
C) a polyploidy cell. 
D) a hapl...
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Molecular Diagnostics Chapter 7 Exam with verified solutions
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Molecular Diagnostics Chapter 7 Exam with 
verified solutions 
How many base pairs are in the human genome? - answer2.9 billion 
What is the difference between a mutation and a polymorphism? - 
answermutations are reserved for rare changes in DNA like those found in 
cancer. Polymorphisms are variants that occur in 1-2% of the population and do 
not affect phenotype heavily 
What are the three largest and smallest chromosomes? - answerlargest: 1, 2 3 
smallest: 22, Y, 19 
What is an example of a...
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PENN FOSTER BIOLOGY: Genetics and Inheritance Exam Questions and Answers 100% Solved
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PENN FOSTER BIOLOGY: Genetics and 
Inheritance Exam Questions and 
Answers 100% Solved 
Trisomy - having three copies of a chromosome instead of two 
euploid - organism with the appropriate number of chromosomes 
Aneuploid - organism with more or less chromosomes inappropriate for 
species 
X inactivation - organism has too many X chromosomes, so one is 
inactivated, not expressed 
Barr bodies - inactive extra X chromosome 
complex traits - genes interact to give rise to different phenotypes 
mu...
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Pathophysiology Exam 1 Questions and Answers
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Pathophysiology Exam 1 Questions and Answers 
An ordered photographic display of a set of chromosomes from a single cell is a(n): 
A) metaphase spread. 
B) autosomal spread. 
C) karyotype. 
D) anaphase spread. - Answer-c 
An error in which homologous chromosomes fail to separate during meiosis is termed: 
A) aneuploidy. 
B) nondisjunction. 
C) polyploidy. 
D) anaplasia. - Answer-b 
A somatic cell that does not contain a multiple of 23 chromosomes is called: 
A) an aneuploid cell. 
B) a euploid c...
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Molecular Diagnostics Chapter 7 100% Solved
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Molecular Diagnostics Chapter 7 100% 
Solved 
How many base pairs are in the human genome? - answer2.9 billion 
What is the difference between a mutation and a polymorphism? - 
answermutations are reserved for rare changes in DNA like those found in 
cancer. Polymorphisms are variants that occur in 1-2% of the population and do 
not affect phenotype heavily 
What are the three largest and smallest chromosomes? - answerlargest: 1, 2 3 
smallest: 22, Y, 19 
What is an example of a balanced polymor...
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Molecular Diagnostics Chapter 7 Exam with verified solutions
- Tentamen (uitwerkingen) • 6 pagina's • 2024
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Molecular Diagnostics Chapter 7 Exam with 
verified solutions 
How many base pairs are in the human genome? - answer2.9 billion 
What is the difference between a mutation and a polymorphism? - 
answermutations are reserved for rare changes in DNA like those found in 
cancer. Polymorphisms are variants that occur in 1-2% of the population and do 
not affect phenotype heavily 
What are the three largest and smallest chromosomes? - answerlargest: 1, 2 3 
smallest: 22, Y, 19 
What is an example of a...
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Test Bank for SueE. Huether Kathryn L. McCance for Understanding Pathophysiology 6thEd. Questions with 100 correct and verified answers with rationale.
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Chapter 01: Cellular Biology Huether & McCance: Understanding Pathophysiology, 6th Edition 
 
 
MULTIPLE CHOICE 
 
1.	A student is observing a cell under the microscope. It is observed to have supercoiled DNA with histones. Which of the following would also be observed by the student? a. A single circular chromosome 
b.	A nucleus 
c.	Free-floating nuclear material 
d.	No organelles 
 
 
ANS: B 
The cell described is a eukaryotic cell, so it has histones and a supercoiled DNA within i...
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