SubstitutionIntronPromoterKlinefelter'sSyndromePraderWilliSyndromeSilentMutationmicroRNANF-2GeneQuantitativePCRKaryotypingDown'sSyndromeMeioticNondisjunctionExonEnhancerTSC-1(TuberousSclerosisGene-1)TurnerSyndromeWilson'sDiseaseHeterochromatinAutosomalRecessiveTranscriptionEuchromatinNF1PenetranceLocusHeterogeneityRobertsonianTranslocationPleiotropyInversionHistoneAcetylationNon-sensemutationDNAMethylationFragile XSyndromeAutosomalDominantCodominanceFISHGeneticAnticipationExcessCAGRepeatsLinkageAnalysisHistoneMethylationGWASAcuteIntermittentPorphyriaSingleNucleotidePolymorphismMis-sensemutationTranslocationSubstitutionIntronPromoterKlinefelter'sSyndromePraderWilliSyndromeSilentMutationmicroRNANF-2GeneQuantitativePCRKaryotypingDown'sSyndromeMeioticNondisjunctionExonEnhancerTSC-1(TuberousSclerosisGene-1)TurnerSyndromeWilson'sDiseaseHeterochromatinAutosomalRecessiveTranscriptionEuchromatinNF1PenetranceLocusHeterogeneityRobertsonianTranslocationPleiotropyInversionHistoneAcetylationNon-sensemutationDNAMethylationFragile XSyndromeAutosomalDominantCodominanceFISHGeneticAnticipationExcessCAGRepeatsLinkageAnalysisHistoneMethylationGWASAcuteIntermittentPorphyriaSingleNucleotidePolymorphismMis-sensemutationTranslocation

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