Campbell Essential Biology with Physiology (5th Edition)
Campbell Essential Biology with Physiology (5th Edition)
5th Edition
ISBN: 9780321967671
Author: Eric J. Simon, Jean L. Dickey, Jane B. Reece, Kelly A. Hogan
Publisher: PEARSON
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Chapter 9, Problem 19PS
Summary Introduction

To explain: The mother’s genotype when the father is deaf, has a double recessive dd genotype, and all the children have hearing capability.

Concept introduction: Genotype is the allelic identity of the organism based on which the phenotype is expressed. Autosomal recessive disorder is where the homozygous or double recessive nature of alleles of the autosomal genes or somatic genes causes defects in the individual, which can range from acute level to chronic level.

Summary Introduction

To explain: The mother’s genotype if the couple has four children (non twins), and all have hearing capabilities.

Concept introduction: Genotype is the allelic identity of the organism based on which the phenotype is expressed. Autosomal recessive disorder is where the homozygous or double recessive nature of alleles of the autosomal genes or somatic genes causes defects in the individual, which can range from acute level to chronic level.

Summary Introduction

To explain: The way in which the genotypes can be assigned.

Concept introduction: Genotype is the allelic identity of the organism based on which the phenotype is expressed. Autosomal recessive disorder is where the homozygous or double recessive nature of alleles of the autosomal genes or somatic genes causes defects in the individual, which can range from acute level to chronic level.

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In humans, an X-linked disorder called coloboma iridia (a fissure in the iris_ is a recessive trait. A normal couple has an afflicted daughter. What would be the most plausible scenario for this situation?   the female is not the biological mother, but the male is the biological father   the father carries one recessive allele, and the mother carries one recessive allele   the mother carries two recessive alleles   the male is not the biological father, but the female is the biological mother   both parents are heterozygous for the trait
The allele for color-blindness is carried on the X chromosome. Making color blindness (a recessive trait) an X - linked trait. A colorblind make and a carrier female for color blindness. (But is not colorblind herself) have a child. Show your work! A) what is the % chance that their son will be color blind? B) what is the % chance that their daughter will be color blind?
Color-blindness is an X-linked recessive disorder. Under what circumstances will this condition manifest in a child?  Top of Form   If the child is a male and its mother has the recessive allele   If the child is a female and its father has the recessive allele   If the child is a female and its mother has the recessive allele   If the child is a male and its father has the recessive allele
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