NF1AutosomalDominantPleiotropySubstitutionHistoneAcetylationSingleNucleotidePolymorphismTranscriptionGWASFragile XSyndromeExonHistoneMethylationmicroRNADown'sSyndromePromoterRobertsonianTranslocationTurnerSyndromeDNAMethylationTranslocationQuantitativePCRNF-2GeneLinkageAnalysisPenetranceKaryotypingIntronExcessCAGRepeatsAutosomalRecessiveFISHGeneticAnticipationWilson'sDiseaseEnhancerTSC-1(TuberousSclerosisGene-1)PraderWilliSyndromeAcuteIntermittentPorphyriaNon-sensemutationCodominanceInversionMeioticNondisjunctionEuchromatinKlinefelter'sSyndromeHeterochromatinLocusHeterogeneitySilentMutationMis-sensemutationNF1AutosomalDominantPleiotropySubstitutionHistoneAcetylationSingleNucleotidePolymorphismTranscriptionGWASFragile XSyndromeExonHistoneMethylationmicroRNADown'sSyndromePromoterRobertsonianTranslocationTurnerSyndromeDNAMethylationTranslocationQuantitativePCRNF-2GeneLinkageAnalysisPenetranceKaryotypingIntronExcessCAGRepeatsAutosomalRecessiveFISHGeneticAnticipationWilson'sDiseaseEnhancerTSC-1(TuberousSclerosisGene-1)PraderWilliSyndromeAcuteIntermittentPorphyriaNon-sensemutationCodominanceInversionMeioticNondisjunctionEuchromatinKlinefelter'sSyndromeHeterochromatinLocusHeterogeneitySilentMutationMis-sensemutation

PRITE GENETICS - Call List

(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.


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  1. NF1
  2. Autosomal Dominant
  3. Pleiotropy
  4. Substitution
  5. Histone Acetylation
  6. Single Nucleotide Polymorphism
  7. Transcription
  8. GWAS
  9. Fragile X Syndrome
  10. Exon
  11. Histone Methylation
  12. microRNA
  13. Down's Syndrome
  14. Promoter
  15. Robertsonian Translocation
  16. Turner Syndrome
  17. DNA Methylation
  18. Translocation
  19. Quantitative PCR
  20. NF-2 Gene
  21. Linkage Analysis
  22. Penetrance
  23. Karyotyping
  24. Intron
  25. Excess CAG Repeats
  26. Autosomal Recessive
  27. FISH
  28. Genetic Anticipation
  29. Wilson's Disease
  30. Enhancer
  31. TSC-1 (Tuberous Sclerosis Gene-1)
  32. Prader Willi Syndrome
  33. Acute Intermittent Porphyria
  34. Non-sense mutation
  35. Codominance
  36. Inversion
  37. Meiotic Nondisjunction
  38. Euchromatin
  39. Klinefelter's Syndrome
  40. Heterochromatin
  41. Locus Heterogeneity
  42. Silent Mutation
  43. Mis-sense mutation