Substitution Intron Promoter Klinefelter's Syndrome Prader Willi Syndrome Silent Mutation microRNA NF-2 Gene Quantitative PCR Karyotyping Down's Syndrome Meiotic Nondisjunction Exon Enhancer TSC-1 (Tuberous Sclerosis Gene-1) Turner Syndrome Wilson's Disease Heterochromatin Autosomal Recessive Transcription Euchromatin NF1 Penetrance Locus Heterogeneity Robertsonian Translocation Pleiotropy Inversion Histone Acetylation Non- sense mutation DNA Methylation Fragile X Syndrome Autosomal Dominant Codominance FISH Genetic Anticipation Excess CAG Repeats Linkage Analysis Histone Methylation GWAS Acute Intermittent Porphyria Single Nucleotide Polymorphism Mis- sense mutation Translocation Substitution Intron Promoter Klinefelter's Syndrome Prader Willi Syndrome Silent Mutation microRNA NF-2 Gene Quantitative PCR Karyotyping Down's Syndrome Meiotic Nondisjunction Exon Enhancer TSC-1 (Tuberous Sclerosis Gene-1) Turner Syndrome Wilson's Disease Heterochromatin Autosomal Recessive Transcription Euchromatin NF1 Penetrance Locus Heterogeneity Robertsonian Translocation Pleiotropy Inversion Histone Acetylation Non- sense mutation DNA Methylation Fragile X Syndrome Autosomal Dominant Codominance FISH Genetic Anticipation Excess CAG Repeats Linkage Analysis Histone Methylation GWAS Acute Intermittent Porphyria Single Nucleotide Polymorphism Mis- sense mutation Translocation
(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.
Substitution
Intron
Promoter
Klinefelter's Syndrome
Prader Willi Syndrome
Silent Mutation
microRNA
NF-2 Gene
Quantitative PCR
Karyotyping
Down's Syndrome
Meiotic Nondisjunction
Exon
Enhancer
TSC-1 (Tuberous Sclerosis Gene-1)
Turner Syndrome
Wilson's Disease
Heterochromatin
Autosomal Recessive
Transcription
Euchromatin
NF1
Penetrance
Locus Heterogeneity
Robertsonian Translocation
Pleiotropy
Inversion
Histone Acetylation
Non-sense mutation
DNA Methylation
Fragile X Syndrome
Autosomal Dominant
Codominance
FISH
Genetic Anticipation
Excess CAG Repeats
Linkage Analysis
Histone Methylation
GWAS
Acute Intermittent Porphyria
Single Nucleotide Polymorphism
Mis-sense mutation
Translocation