Monosomy Study guides, Class notes & Summaries
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CPN Exam Questions and Answers 100% Correct(RATED A+)
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monosomy - ANSWER-the loss of one chromosome from a pair; usually rare & fetus is usually non-viable 
 
trisomy - ANSWER-an addition to a pair of chromosomes; relatively common 
 
autosomal dominant inheritance - ANSWER-children of a heterozygous parent have a 50% chance of possessing the defective gene. children who don't inherit the defective gene will themselves have unaffected offspring. 
 
examples of autosomal dominant disorders (2) - ANSWER-marfan syndrome & neurofibromatosis 
 
autosoma...
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Chapter 31 Care of the Child With a Physical and Mental or Cognitive Disorders
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Chapter 31 Care of the Child With a Physical and Mental or Cognitive Many of the health problems that affect children differ from those of adults, and 
management of these problems can be quite different as well. Nurses need to be aware of 
the unique way they provide care to children and their families. In providing nursing 
interventions to children, it is important to include parents as much as possible, delegating 
to them any interventions that are appropriate. It is also necessary to provi...
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024.
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024. 
1. A baby is born with what the physician believes is a diagnosis of trisomy 21. This means that the 
infant has three number 21 chromosomes. What factor describes the etiology of this genetic 
change? 
a. The mother also has genetic mutation of chromosome 21. 
b. The patient has a nondisjunction occurring during meiosis. 
c. During meiosis, a reduction of chromosomes resulted in 23. 
d. The patie...
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024.
- Exam (elaborations) • 21 pages • 2024
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024. 
1. A baby is born with what the physician believes is a diagnosis of trisomy 21. This means that the 
infant has three number 21 chromosomes. What factor describes the etiology of this genetic 
change? 
a. The mother also has genetic mutation of chromosome 21. 
b. The patient has a nondisjunction occurring during meiosis. 
c. During meiosis, a reduction of chromosomes resulted in 23. 
d. The patie...
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Exam 2 genetics portage learning 2023 complete study guide
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Exam 2 Genetics 
Chapter 7 
 Nondisjunction in meiosis – can cause XXX Syndrome or XYY Condition 
 47 XYY – famous 
o There’s this idea that there is an over representation of XYY of men in prison 
o Some people think that people with XYY are more likely to become criminals or 
get put in jail 
o Above average in height and below average in intelligence 
 Sex determination 
o At 5 or 6 weeks there is a potential for the fetus to get a Y chromosome and 
become a male 
 PAR: pseu...
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024.
- Exam (elaborations) • 21 pages • 2024
- Available in package deal
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024. 
1. A baby is born with what the physician believes is a diagnosis of trisomy 21. This means that the 
infant has three number 21 chromosomes. What factor describes the etiology of this genetic 
change? 
a. The mother also has genetic mutation of chromosome 21. 
b. The patient has a nondisjunction occurring during meiosis. 
c. During meiosis, a reduction of chromosomes resulted in 23. 
d. The patie...
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PATHOPHYSIOLOGY EXAM / TEST BANK 2023 LATEST EDITION,VERIFIED QUESTIONS AND ANSWERS GRADED A+.
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PATHOPHYSIOLOGY EXAM / TEST BANK 2023 LATEST EDITION,VERIFIED QUESTIONS AND ANSWERS GRADED A+. 
 
 
 
1.	Which of the following assessment findings indicates an altercation in homeostatic control mechanisms? 
 
 
A.	Fever 
B.	Throat Pain 
 Joint Stiffness 
C.	Positive throat culture: A. Fever 
2.	While assessing a patient diagnosed with Marfan's Syndrome the nurse should include which of the following is consistent with the syndrome: 
A.	cardiac assessment for coarctation of the aorta 
B.	gen...
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PCB 3036 Key PASSED Exam Questions and CORRECT Answers
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Trisomy vs Monosomy Trisomy - a gain of a single chromosome 
Monosomy - loss of a single chromosome 
aneuploidy -gain or loss of a single chromosome 
-result is an imbalance in gene copy number 
study pics in camera roll do it now 
Nondisjunction -Error during gamete formation in meiosis 
-Failure of the chromosome, when lined up at the metaphase plate, to pull apart. Can occur in 
first or second meiotic division.
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Chapter 03: Hereditary Influences on Health Promotion of the Child and Family Test Bank for Wong's Nursing Care of Infants And Children 11th Edition by Hockenberry
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TEST BANK FOR WONG'S NURSING CARE OF INFANTS AND CHILDREN 11TH EDITION BY HOCKENBERRY 
 
Chapter 03: Hereditary Influences on Health Promotion of the Child and Family 
 
MULTIPLE CHOICE 
 
1.	Which genetic term refers to a person who possesses one copy of an affected gene and one copy of an unaffected gene and is clinically unaffected? 
a.	Allele 
b.	Carrier 
c.	Pedigree 
d.	Multifactorial 
ANS: B 
An individual who is a carrier is asymptomatic but possesses a genetic alteration, either in the ...
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NSG 530 Advanced Pathophysiology STUDY GUIDE PATHO QUIZ 1 LATEST QUESTIONS WITH CORRECT SOLUTIONS PASSED A+ VERIFIED
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Human cell can be categorized into gametes (Sperm & egg cells) and somatic cells, which include 
all cells other than gametes. Each somatic cell nucleus has 46 chromosomes in 23 pairs. These are 
diploid cells, and the individual’s fatherand mother each donate on chromosome per pair. New 
somatic cells are formed through mitosis and cytokinesis. 
Gametes are haploid cells: they have only 1 member of each chromosome pair, for a total of 23 
chromosomes. Haploidcells are formed from diploid cel...
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