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