BIOL 107 LAB PKG W/LAB SG +ACCESS >IC<
12th Edition
ISBN: 9781259827082
Author: Mader
Publisher: MCGRAW-HILL HIGHER EDUCATION
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Chapter 11.3, Problem 1CYP
Summarize how to distinguish an autosomal recessive disorder from an autosomal dominant disorder using a pedigree.
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Describe the characteristics of a pedigree for an autosomal dominant and an autosomal recessive trait.
Draw a family tree or pedigree showing the difference in inheritance between an autosomal dominant disorder and an autosomal recessive disorder.
List the characteristics of autosomal dominant and autosomal recessive pedigrees.
Chapter 11 Solutions
BIOL 107 LAB PKG W/LAB SG +ACCESS >IC<
Ch. 11.1 - Explain the difference between the particulate...Ch. 11.1 - Explain why the garden pea was a good choice for...Ch. 11.2 - Summarize how Mendel's laws of independent...Ch. 11.2 - Explain why the Tt and TT genotypes both have the...Ch. 11.2 - Calculate the probability of producing an Aabb...Ch. 11.3 - Summarize how to distinguish an autosomal...Ch. 11.3 - 2. Construct a pedigree of Ivar Ragnarsson's...Ch. 11.4 - Prob. 1CYPCh. 11.4 - Prob. 2CYPCh. 11.4 - Prob. 3CYP
Ch. 11 - How may a pedigree pattern be used to determine if...Ch. 11 - Prob. 1NS.2QCCh. 11 - Prob. 1ACh. 11 - Prob. 2ACh. 11 - Prob. 3ACh. 11 - In peas, yellow seed (h is dominant over green...Ch. 11 - 5. In guinea pigs, smooth coat (S) is dominant...Ch. 11 - In horses,B= black coat,b= brown coat,T= trotter,...Ch. 11 - Prob. 7ACh. 11 - Cystic fibrosis is an example of a/an trait. a....Ch. 11 - Prob. 9ACh. 11 - Prob. 10ACh. 11 - Prob. 11ACh. 11 - Prob. 12ACh. 11 - Prob. 13ACh. 11 - Prob. 14ACh. 11 - Prob. 1TSCh. 11 - Prob. 2TSCh. 11 - Prob. 3TSCh. 11 - Prob. 4TS
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- Assume for a moment that a child has a autosomal recessive disorder, but both parents appear normal. What is the genotype of both parents? : one parent must be homozygous dominant : both parents must be homozygous recessive : both parents are heterozygous : both parents nust be homozygous dominantarrow_forwardWhich genotype indicates a carrier of an autosomal recessive trait? bb BB Bbarrow_forwardHuntington disease (HD) is a genetic disorder that usually first appears in middle age and, over time, leads to involuntary movements, impaired speech, difficulty swallowing and speaking, and cognitive decline. There is no cure for HD, and affected individuals eventually die, usually after 10 to 15 years of progressively worsening symptoms. Huntington disease is inherited as an autosomal dominant disorder. Presymptomatic genetic testing for HD is available for people with a family history of the disease. Individuals who have a parent with HD have a 50% chance of inheriting the HD gene and eventually having HD. Some of these individuals want to know if they will eventually get the disease, and they undergo presymptomatic genetic testing. Others do not want to know, given that there is no cure or effective treatment for the disease. If you were at risk for HD, would you want to undergo genetic testing? What are some reasons for and against having a genetic test for HD?arrow_forward
- . Recognize autosomal dominant and autosomal recessivepatterns of inheritance when examining a pedigree.arrow_forwardDistinguish between autosomal recessive and autosomaldominant genetic disorders.arrow_forwardChoose a pattern of inheritance (autosomal recessive, X-linked dominant, etc.) and identify a disorder with that inheritance pattern. Explain how using a pedigree will help a family understand their probability of passing or inheriting the disorder.arrow_forward
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