Human Biology
16th Edition
ISBN: 9781260482799
Author: Mader, Sylvia
Publisher: MCGRAW-HILL HIGHER EDUCATION
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Chapter 19.6, Problem 2CYP
Summary Introduction
To analyze:
Describe the chromosomal abnormality associated with Down syndrome.
Introduction:
Nondisjunction is the failure of separation of homologous chromosomes or sister chromatids during anaphase I and anaphase II respectively. It results in the presence of an abnormal number of chromosomes in the progeny.
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List the genetic disorders resulting from chromosome deletions:
Explain how it is possible for a person with a translocationor an inversion to be phenotypically normal.
Discuss the mechanisms that lead to erroneous chromosome duplication, mention how they effect the development of Down’s syndrome.
Chapter 19 Solutions
Human Biology
Ch. 19.1 - Distinguish between a chromosome and chromatin.Ch. 19.1 - Prob. 2LOCh. 19.1 - Prob. 3LOCh. 19.1 - Prob. 1CYPCh. 19.1 - Prob. 2CYPCh. 19.1 - Prob. 3CYPCh. 19.2 - Prob. 1LOCh. 19.2 - Prob. 2LOCh. 19.2 - Prob. 3LOCh. 19.2 - Describe the cell cycle, and list the locations of...
Ch. 19.2 - Prob. 2CYPCh. 19.2 - Prob. 3CYPCh. 19.2 - Summarize why external controls may be necessary...Ch. 19.3 - Prob. 1LOCh. 19.3 - Prob. 2LOCh. 19.3 - Prob. 3LOCh. 19.3 - Prob. 1CYPCh. 19.3 - Prob. 2CYPCh. 19.3 - Prob. 3CYPCh. 19.4 - Prob. 1LOCh. 19.4 - Prob. 2LOCh. 19.4 - Prob. 3LOCh. 19.4 - Prob. 1CYPCh. 19.4 - Explain how meiosis reduces the likelihood that...Ch. 19.4 - Prob. 3CYPCh. 19.4 - Compare and contrast the stages of oogenesis and...Ch. 19.5 - Prob. 1LOCh. 19.5 - Prob. 2LOCh. 19.5 - List the similarities and differences between...Ch. 19.5 - Prob. 2CYPCh. 19.5 - Prob. 3CYPCh. 19.6 - Prob. 1LOCh. 19.6 - Describe the causes and consequences of trisomy...Ch. 19.6 - Prob. 3LOCh. 19.6 - 4. Describe the effects of deletions,...Ch. 19.6 - Prob. 1BTSCh. 19.6 - Prob. 2BTSCh. 19.6 - Prob. 1CYPCh. 19.6 - Prob. 2CYPCh. 19.6 - Prob. 3CYPCh. 19.6 - Prob. 4CYPCh. 19 - Prob. 1ACh. 19 - 2. Which of the following is/are produced by the...Ch. 19 - 3. Label the drawing of the cell cycle: then list...Ch. 19 - 4. At which of the following checkpoints is the...Ch. 19 - ...Ch. 19 - ...Ch. 19 - a. metaphase
b....Ch. 19 - ...Ch. 19 - metaphase
prornetaphase
telophase
prophase c....Ch. 19 - 10. If a parent cell has a diploid number of 18...Ch. 19 - 11. If a parent cell has 22 chromosomes. the...Ch. 19 - 12. Crossing-over occurs between
sister chromatids...Ch. 19 - 13. Which of these helps provide genetic...Ch. 19 - 14. Polar bodies are produced during
DNA...Ch. 19 - 15. The pairing of homologous chromosomes occurs...Ch. 19 - 16. Sister chromatids separate during anaphase of...Ch. 19 - 17. Monosomy or trisomy occurs because...Ch. 19 - 18. A person with Klinefelter syndrome is and...Ch. 19 - Prob. 1TCCh. 19 - Prob. 2TCCh. 19 - Prob. 3TCCh. 19 - Prob. 4TC
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- Describe a chromosomal deletion, duplication, translocation, and inversion.arrow_forwardIdentify the type of chromosomal aberration described in each of the following cases and provide and example. loss of a chromosome segment extra copies of a chromosome segment reversal in the order of a chromosome segment movement of a chromosome segment to another, non homologous chromosomearrow_forwardexplain the Phenotypic effects of duplicationsarrow_forward
- Describe the chromosomal alterations and phenotype of cri du chat syndrome and Prader-Willi syndrome.arrow_forwardIll.siven the following pedigree below, use Punnett squares for each of the following possibilities: a) X- linked dominant, b) X-linked recessive, c) Autosomal dominant and d) Autosomal recessive in order to determine what is the mode of transmission of this trait. Disease allele = Xª, x², A or a depending on mode of transmission of the disease respectively. Unaffected X chromosome = X *Homozygous unaffected/No 1 *2 carrier=Normal II 1 *4 1 2 3 6. 7 8 a) X-linked dominant 11x12 b) X-linked recessive I 1 x1 2 c) Autosomal dominant 11x12 d) Autosomal recessive I1x12 IV. Based on your analysis what is the mode of transmission for this disease? O+arrow_forwardGive bilological term for an alternation in the genetic material that can be inherited.arrow_forward
- What is the Philadelphia chromosome? How is this chromosome related to cancer? Identify how this chromosome appears physically different in a karyotype than it appears in a normal karyotype. Include references to information sources used.arrow_forwardExplain the reason why a dicentric chromosome is unstable.arrow_forwardWhat is chromosome disorder explain with examples.arrow_forward
- b. Why were the people with the translocation less severely affected than the people with the microdeletion? c. What other problems might arise in the family with the translocation?arrow_forwardWhat are some physical appearances of individuals affected by the abnormality structure of deletion, inversion, duplication, and translocation?arrow_forwardExamine the karyotypes of Jacob and PAtau syndromes. List the similarities and differences between these two syndromes. which is more severe?arrow_forward
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