Nondisjunction - Study guides, Class notes & Summaries

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Test bank for Applied Pathophysiology for the Advanced Practice Nurse 2nd Edition by Dlugasch and Story (STUVIA) Test bank for Applied Pathophysiology for the Advanced Practice Nurse 2nd Edition by Dlugasch and Story (STUVIA)
  • Test bank for Applied Pathophysiology for the Advanced Practice Nurse 2nd Edition by Dlugasch and Story (STUVIA)

  • Exam (elaborations) • 138 pages • 2024
  • Test bank for Applied Pathophysiology for the Advanced Practice Nurse 2nd Edition by Dlugasch and Story (STUVIA) Applied Pathophysiology for the Advanced Practice Nurse, Second Edition by Dlugasch and Story Sample Questions: Chapter 1 Assessment Quiz Import Settings: Base Settings: Brownstone Default Information Field: Complexity Information Field: Ahead Information Field: Subject Information Field: Title Information Field: Feedback Information Field: Taxonomy Information Field: Object...
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Pathophysiology Exam 1 questions and answers all are graded A+
  • Pathophysiology Exam 1 questions and answers all are graded A+

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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 haploid cell...
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WGU D115 FINAL EXAM STUDY GUIDE 2024/ACTUAL EXAM QUESTIONS WITH CORRECT VERIFIED ANSWERS/100% PASS GUARANTEE
  • WGU D115 FINAL EXAM STUDY GUIDE 2024/ACTUAL EXAM QUESTIONS WITH CORRECT VERIFIED ANSWERS/100% PASS GUARANTEE

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  • WGU D115 FINAL EXAM STUDY GUIDE 2024/ACTUAL EXAM QUESTIONS WITH CORRECT VERIFIED ANSWERS/100% PASS GUARANTEE What is the most common cause of down syndrome - Maternal nondisjunction What syndrome characterized by absent homologous X chromosome With only a single X- chromosome Exhibit features include Short stature Widely spaced nipples And webbed neck - Turner syndrome
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024.
  • 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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Pathophysiology Exam Question and answers  2024 verified to pass
  • Pathophysiology Exam Question and answers 2024 verified to pass

  • Exam (elaborations) • 47 pages • 2024
  • Pathophysiology Exam Question and answers 2024 verified to passPathophysiology Exam 1 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. - correct answer c An error in which homologous chromosomes fail to separate during meiosis is termed: A) aneuploidy. B) nondisjunction. C) polyploidy. D) anaplasia. - correct answer b A somatic cell that does not contain a multiple...
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ABGC 100 Genetic Conditions Exam With 100% Correct And Verified Answers
  • ABGC 100 Genetic Conditions Exam With 100% Correct And Verified Answers

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  • ABGC 100 Genetic Conditions Exam With 100% Correct And Verified Answers T13 - Correct Answer-Nondisjunction; 1 in 12,000 SGA, MCA: hypotelorism, CLP, heart, brain and kidney defects RR is 1% T18 - Correct Answer-Nondisjunction; 1 in 6,000 SGA, MCA: prominent occiput, tightly clenched fingers, heart and brain defects Choroid plexus cyst on u/s RR is 1% T21 - Correct Answer-MATERNAL nondisjunction (90%); 5% translocation 21;**usually 14**; 2% mosaic T21 1 in 800 Hypotonic, heart (50...
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2024 ASU BIO 340 EXAM 3 FINAL EXAM WITH WELL ARRANGED QUESTIONS & COMPLETE 100% CORRECTLY VERIFIED  ANSWERS WITH RATIONALES WELL EXPLAINED BY EXPERTS AND GRADED A+ 2024 LATEST UPDATE ALREADY PASSED!!!!!! WITH 100% GUARANTEED PASS AFTER DOWNLOAD (ALL YOU N
  • 2024 ASU BIO 340 EXAM 3 FINAL EXAM WITH WELL ARRANGED QUESTIONS & COMPLETE 100% CORRECTLY VERIFIED ANSWERS WITH RATIONALES WELL EXPLAINED BY EXPERTS AND GRADED A+ 2024 LATEST UPDATE ALREADY PASSED!!!!!! WITH 100% GUARANTEED PASS AFTER DOWNLOAD (ALL YOU N

  • Exam (elaborations) • 68 pages • 2024
  • 2024 ASU BIO 340 EXAM 3 FINAL EXAM WITH WELL ARRANGED QUESTIONS & COMPLETE 100% CORRECTLY VERIFIED ANSWERS WITH RATIONALES WELL EXPLAINED BY EXPERTS AND GRADED A+ 2024 LATEST UPDATE ALREADY PASSED!!!!!! WITH 100% GUARANTEED PASS AFTER DOWNLOAD (ALL YOU NEED TO EXCEL IN YOUR STUDIES What is the mammalian transcription factor that elicits a cascade of gene transcription and developmental events that ultimately produce male internal and external structures? SRY If a trait is X-linked recessive,...
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Pathophysiology Certification Exam  Questions And CORRECT Answers
  • Pathophysiology Certification Exam Questions And CORRECT Answers

  • Exam (elaborations) • 39 pages • 2024
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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.c An error in which homologous chromosomes fail to separate during meiosis is termed: A) aneuploidy. B) nondisjunction. C) polyploidy. D) anaplasia.b
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CMMB 413 MT 2 Question and answers correctly solved 2024
  • CMMB 413 MT 2 Question and answers correctly solved 2024

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  • CMMB 413 MT 2 Question and answers correctly solved 2024 Underlying mechanism of abnormal chromosome segregation: - correct answer Nondisjunction Underlying mechanism of recurrent chromosome syndromes: - correct answer Recombination at segmental duplications Underlying mechanism of idiopathic chromosome abnormalities: - correct answer Sporadic, variable breakpoints Spontaneous/de novo. Sometimes of unknown origin. - correct answer Idiopathic Underlying mechanism of unbalanced f...
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ATI Med Surg Test Questions Overview of Genetics and Genomics in Nursing 100%Correct Answers 2024.
  • 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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