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Chapter 3

Quiz yourself by thinking what should be in each of the black spaces below before clicking on it to display the answer.
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Question
Answer
DNA (deoxyribonucleic acid)   show
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show One of the 46 molecules of DNA 9 (in 23 pairs) that virtually each cell of the human body contains and that together, contain all the genes. Other species have more or fewer chromosomes.  
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show A small section of a chromosome; the basic unit for the transmission of heredity. A gene consists of a string of chemicals that provide instructions for the cell to manufacture certain proteins.  
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show A variation that makes a gene different in some way from other genes for the same characteristics. Many genes never vary; others have several possible alleles.  
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Genome   show
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Zygote   show
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show A reproductive cell; that is a sperm or ovum that can produce a new individual if it combines with a gamete from the other sex to make a zygote.  
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show An organism's entire genetic inheritance, or genetic potential.  
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show Referring to two genes of one pair that are exactly the same in every letter of their code. Most gene pairs are homozygous.  
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23rd Pair   show
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XX   show
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XY   show
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Stem Cells   show
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show Twins who originate from one zygote that splits apart very early in development. (a.k.a identical twins). Other monozygotic multiple births (such as triplets) can occur.  
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Dizygotic Twins   show
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show A general term for the techniques designed to help infertile couples conceive and then sustain a pregnancy.  
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In Vitro Fertilization (IVF)   show
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show The observable characteristics of a person, including appearance, personality, intelligence, and all other traits.  
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Multifactorial   show
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show Referring to environment factors that affect genes and genetic expression; enhancing, halting, shaping, or altering the expression of genes, resulting in a phenotype that may differ markedly from the genotype.  
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show Referring to a trait that is influenced by many genes.  
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show An international effort to map the complete human genetic code, This effort was essentially completed in 2001, though analysis is ongoing.  
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Dominant-Recessive Pattern   show
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Carrier   show
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X-linked   show
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Heritability   show
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show A condition in which a person has 47 chromosomes instead of the usual 46, with 3 rather than 2 chromosomes at the 21st site. People with Down syndrome typically have distinctive characteristics, including unusual facial features, heart abnormalities.  
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Huntington disease   show
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show A genetic disorder in which part of the X chromosome seems to be attached to the rest of it by a very thin string of molecules. The cause is a single gene that has more than 200 repetitions of one triplet.  
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show Consultation and testing by trained experts that enable individuals to learn about their genetic heritage, including harmful conditions that they might pass along to any children they may conceive.  
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show A genetic disorder in which a child's body is unable to metabolize an amino acid called phenylalanine. Unless the infant immediately begins a special diet, the resulting buildup of phenylalanine in body fluids causes brain damage.  
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Created by: aglana
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