FileTitleManuscript Id
Chapter 15 Introductionmorris2e_ch15_1.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_1_dlap.xml5612c44e757a2ece66000000
15.1 Genotype and Phenotype morris2e_ch15_2.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_2_dlap.xml5612c44e757a2ece66000000
Genotype is the genetic makeup of a cell or organism; phenotype is its observed characteristics. morris2e_ch15_3.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_3_dlap.xml5612c44e757a2ece66000000
The effect of a genotype often depends on several factors. morris2e_ch15_4.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_4_dlap.xml5612c44e757a2ece66000000
Some genetic differences are major risk factors for disease. morris2e_ch15_5.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_5_dlap.xml5612c44e757a2ece66000000
Not all genetic differences are harmful. morris2e_ch15_6.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_6_dlap.xml5612c44e757a2ece66000000
A few genetic differences are beneficial. morris2e_ch15_7.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_7_dlap.xml5612c44e757a2ece66000000
15.2 Genetic Variation and Individual Uniqueness morris2e_ch15_8.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_8_dlap.xml5612c44e757a2ece66000000
Areas of the genome with variable numbers of tandem repeats are useful in DNA typing. morris2e_ch15_9.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_9_dlap.xml5612c44e757a2ece66000000
Some polymorphisms add or remove restriction sites in the DNA. morris2e_ch15_10.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_10_dlap.xml5612c44e757a2ece66000000
15.3 Genomewide Studies of Genetic Variation morris2e_ch15_11.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_11_dlap.xml5612c44e757a2ece66000000
Single-nucleotide polymorphisms (SNPs) are single-base changes in the genome. morris2e_ch15_12.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_12_dlap.xml5612c44e757a2ece66000000
Case 3: How can genetic risk factors be detected? morris2e_ch15_13.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_13_dlap.xml5612c44e757a2ece66000000
Copy-number variation constitutes a significant proportion of genetic variation. morris2e_ch15_14.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_14_dlap.xml5612c44e757a2ece66000000
15.4 Genetic Variation in Chromosomes morris2e_ch15_15.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_15_dlap.xml5612c44e757a2ece66000000
Nondisjunction in meiosis results in extra or missing chromosomes. morris2e_ch15_16.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_16_dlap.xml5612c44e757a2ece66000000
Some human disorders result from nondisjunction. morris2e_ch15_17.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_17_dlap.xml5612c44e757a2ece66000000
Extra or missing sex chromosomes have fewer effects than extra autosomes. morris2e_ch15_18.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_18_dlap.xml5612c44e757a2ece66000000
Nondisjunction is a major cause of spontaneous abortion. morris2e_ch15_19.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_19_dlap.xml5612c44e757a2ece66000000
Chapter 15 Summarymorris2e_ch15_20.html5612c44e757a2ece66000000
DLAP questionsmorris2e_ch15_20_dlap.xml5612c44e757a2ece66000000