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209 Cards in this Set
- Front
- Back
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SNPs
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single-base differences
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Autosomal Dominant Trait
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a
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Autosomal Recessive Trait
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kj
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X-linked Dominant
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j
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X-Linked Recessive
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j
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Ch square Test
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j
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Tetrad Analysis in Ordered Tetrads
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j
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Tetrad Analysis in Unordered Tetrads
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j
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cM
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j
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Map Distance
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j
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PD
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j
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NPD
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j
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TT
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j
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PD >> NPD
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the 2 genes are genetically linked
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PD = NPD
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the 2 genes are genticallly independent (unlinked)
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Parentals > Recombinants
RF < 50% |
Linked Genes
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Linked genes are usually close or far apart?
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close toegther
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Parentals = Recombinant
RF = 50% |
Unlinked Genes
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Complete Dominance
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Hybrid resembles one of the 2 parents
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Incomplete Dominance
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Hybrid remebles neither parent
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Codominance
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Hbrid shors traits from both parents
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Gene Expression
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h
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Genetics
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j
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Genome
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j
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Haploid
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h
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Haplotype
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j
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Histone
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h
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Homeobox
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h
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Homeodomain
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h
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Imprinting
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h
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Intron
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h
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MicroRNA (miRNA)
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n
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Mutation
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j
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Protein
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j
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Amino Acid
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j
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Chromatin
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j
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Chromosome
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j
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Diploid
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j
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DNA
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j
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Epigenetics
|
j
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Exon
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j
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Gene
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h
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Recombinant DNA
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j
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Ribosome
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j
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RNA
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j
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RNA interferebce (RNAi)
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n
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RNA Polymerase
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j
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RNA splicing
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j
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Alternatice Splicing
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j
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Telomere
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j
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Telomerase
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j
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Transcription
|
j
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Translation
|
j
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Variant
|
j
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Sequencing
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j
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Chaperone Proteins
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j
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Anticodon
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j
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Coding Strand
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j
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Codon
|
j
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Conformatio
|
j
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Genetic Code
|
j
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Nonsynomynous Codon
|
j
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Primary Structure
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j
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Secondary Structure
|
n
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tertiary Structure
|
j
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Quatenerary Structure
|
n
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Promoter
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j
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Proteasome
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j
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Reading Frame
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j
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Synonymous Codons
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j
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Template Strand
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j
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Transcription Factor
|
j
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Uracil
|
j
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Polymorphism
|
j
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Allele
|
j
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Autosome
|
j
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Phenotype
|
k
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Karyotype
|
j
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Multifactoial Trait
|
k
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Mutation
|
j
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Pedigrees
|
n
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SNP
Single Nucleotide Polymorphism |
j
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Apoptosis
|
j
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Cell Cycle
|
k
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Centromere
|
kj
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Centrosome
|
j
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Chromatid
|
j
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Cytokinesis
|
h
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G0
|
j
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G1
|
j
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G2
|
k
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Interphase
|
j
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Ligand
|
j
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Metaphase
|
d
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Nucleic Acid
|
n
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Mitosis
|
j
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mRNA
|
j
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rRNA
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j
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tRNA
|
j
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Prophase
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j
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Protein
|
j
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S phase
|
j
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Somatic Cells
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j
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Germ Line Cells
|
k
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Ribosome
|
j
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Spindle
|
j
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Telomere
|
j
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telophase
|
j
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Cleavage
|
k
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Crossing Over
|
c
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Homologous Pairs
|
j
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Independent Assortment
|
j
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Barr Body
|
j
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Reduction Division
|
j
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Autosomal Dominant
|
j
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Autosomal Recessive
|
j
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Monohydrid Cross
|
j
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Dihybrid Cross
|
j
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Testcross
|
h
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Law of Independent Assortment
|
j
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Law of Segregation
|
j
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Mutant
|
j
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Mutation
|
j
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Pedigree
|
j
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Punnet Squear
|
j
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Wilt Type
|
j
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Codominant
|
k
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Epistasis
|
j
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Expressivity
|
j
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Genetic Heterogenity
|
h
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Heplotype
|
j
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Incomplete Dominance
|
j
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Linkage
|
h
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Penetrance
|
j
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Phenocopy
|
j
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Linkage Map
|
j
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cM
|
k
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Pleiotopic
|
j
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Recombinant
|
j
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Epigenetic
|
j
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Genomic Imprinting
|
j
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Hemizygous
|
k
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Heterogametic Sex
|
j
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Homogametic Sex
|
j
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Sex-Limited Trait
|
j
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Transcription Factor
|
j
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X-inactivation
|
h
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X-linked
|
j
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Y-linked
|
j
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Coefficent of relatedness
|
j
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Heritability
|
j
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Incidence
|
j
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Multifactorial Trait
|
j
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Polygenic traits
|
j
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Prevalence
|
j
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Adenine
|
j
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Antiparallel
|
j
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Chromatin
|
j
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Complementary base pairs
|
j
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Cytosine
|
h
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deoxyribose
|
j
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DNA polmerase
|
j
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Guanine
|
j
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Histon
|
j
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Nucleosome
|
j
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Nucleotide
|
h
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Purine
|
j
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Pyrimidine
|
j
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Replication Fork
|
j
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Ribsose
|
k
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Semiconservative Replication
|
k
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Sugar-Phosphate Backbone
|
j
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Thymine
|
j
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Uracil
|
j
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Chromatin Remodeling
|
j
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Epigenetic
|
j
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microRNA
|
j
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psuedogene
|
j
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Proteomics
|
j
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Gene Pool
|
j
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Hardy-Weinberg Equilibrium
|
j
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Macroevolution
|
j
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Microevoulution
|
j
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Populaiton genetics
|
j
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Polpulation
|
j
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Cenrtomere
|
j
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Euchromatin
|
j
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Heterochromatin
|
j
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Nondisjunction
|
j
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Base Exicion Repair
|
j
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Conditional Mutation
|
j
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Deletion Mtation
|
j
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excision Repair
|
j
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Frameshit Mutation
|
j
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Germiline Mutation
|
j
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Mismatch Repair
|
j
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Missense
|
\s
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Silent Mutation
|
ss
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Nonsense Mutation
|
s
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Nucleotide Excision Repair
|
k
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Point Mutation
|
j
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Somatic Mutation
|
j
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Transition
|
h
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Transvesion
|
j
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Polymorphic
|
j
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Allele Frequency
|
j
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Temperature Sensitive Allele
|
j
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Modifier Gene
|
j
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Attentuation
|
j
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