IntronExonEnhancerAutosomalRecessivePenetranceTurnerSyndromeKaryotypingDNAMethylationTranscriptionPleiotropyHistoneAcetylationFISHLinkageAnalysisExcessCAGRepeatsNon-sensemutationCodominanceMis-sensemutationNF-2GeneLocusHeterogeneityPraderWilliSyndromeAcuteIntermittentPorphyriaInversionMeioticNondisjunctionHeterochromatinKlinefelter'sSyndromeGWASAutosomalDominantSubstitutionHistoneMethylationTSC-1(TuberousSclerosisGene-1)Fragile XSyndromeRobertsonianTranslocationDown'sSyndromeSilentMutationWilson'sDiseasePromoterTranslocationEuchromatinQuantitativePCRNF1SingleNucleotidePolymorphismGeneticAnticipationmicroRNAIntronExonEnhancerAutosomalRecessivePenetranceTurnerSyndromeKaryotypingDNAMethylationTranscriptionPleiotropyHistoneAcetylationFISHLinkageAnalysisExcessCAGRepeatsNon-sensemutationCodominanceMis-sensemutationNF-2GeneLocusHeterogeneityPraderWilliSyndromeAcuteIntermittentPorphyriaInversionMeioticNondisjunctionHeterochromatinKlinefelter'sSyndromeGWASAutosomalDominantSubstitutionHistoneMethylationTSC-1(TuberousSclerosisGene-1)Fragile XSyndromeRobertsonianTranslocationDown'sSyndromeSilentMutationWilson'sDiseasePromoterTranslocationEuchromatinQuantitativePCRNF1SingleNucleotidePolymorphismGeneticAnticipationmicroRNA

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