Intron Exon Enhancer Autosomal Recessive Penetrance Turner Syndrome Karyotyping DNA Methylation Transcription Pleiotropy Histone Acetylation FISH Linkage Analysis Excess CAG Repeats Non- sense mutation Codominance Mis- sense mutation NF-2 Gene Locus Heterogeneity Prader Willi Syndrome Acute Intermittent Porphyria Inversion Meiotic Nondisjunction Heterochromatin Klinefelter's Syndrome GWAS Autosomal Dominant Substitution Histone Methylation TSC-1 (Tuberous Sclerosis Gene-1) Fragile X Syndrome Robertsonian Translocation Down's Syndrome Silent Mutation Wilson's Disease Promoter Translocation Euchromatin Quantitative PCR NF1 Single Nucleotide Polymorphism Genetic Anticipation microRNA Intron Exon Enhancer Autosomal Recessive Penetrance Turner Syndrome Karyotyping DNA Methylation Transcription Pleiotropy Histone Acetylation FISH Linkage Analysis Excess CAG Repeats Non- sense mutation Codominance Mis- sense mutation NF-2 Gene Locus Heterogeneity Prader Willi Syndrome Acute Intermittent Porphyria Inversion Meiotic Nondisjunction Heterochromatin Klinefelter's Syndrome GWAS Autosomal Dominant Substitution Histone Methylation TSC-1 (Tuberous Sclerosis Gene-1) Fragile X Syndrome Robertsonian Translocation Down's Syndrome Silent Mutation Wilson's Disease Promoter Translocation Euchromatin Quantitative PCR NF1 Single Nucleotide Polymorphism Genetic Anticipation microRNA
(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.
Intron
Exon
Enhancer
Autosomal Recessive
Penetrance
Turner Syndrome
Karyotyping
DNA Methylation
Transcription
Pleiotropy
Histone Acetylation
FISH
Linkage Analysis
Excess CAG Repeats
Non-sense mutation
Codominance
Mis-sense mutation
NF-2 Gene
Locus Heterogeneity
Prader Willi Syndrome
Acute Intermittent Porphyria
Inversion
Meiotic Nondisjunction
Heterochromatin
Klinefelter's Syndrome
GWAS
Autosomal Dominant
Substitution
Histone Methylation
TSC-1 (Tuberous Sclerosis Gene-1)
Fragile X Syndrome
Robertsonian Translocation
Down's Syndrome
Silent Mutation
Wilson's Disease
Promoter
Translocation
Euchromatin
Quantitative PCR
NF1
Single Nucleotide Polymorphism
Genetic Anticipation
microRNA