SilentMutationLinkageAnalysisHeterochromatinPromoterHistoneMethylationLocusHeterogeneityPleiotropyEnhancerFragile XSyndromeTurnerSyndromeCodominanceAutosomalDominantSingleNucleotidePolymorphismTranscriptionDNAMethylationGeneticAnticipationTSC-1(TuberousSclerosisGene-1)PraderWilliSyndromeRobertsonianTranslocationWilson'sDiseaseEuchromatinNF-2GenePenetranceNF1ExcessCAGRepeatsTranslocationNon-sensemutationMeioticNondisjunctionAutosomalRecessiveGWASFISHSubstitutionIntronKaryotypingKlinefelter'sSyndromeDown'sSyndromeQuantitativePCRMis-sensemutationHistoneAcetylationExonInversionmicroRNAAcuteIntermittentPorphyriaSilentMutationLinkageAnalysisHeterochromatinPromoterHistoneMethylationLocusHeterogeneityPleiotropyEnhancerFragile XSyndromeTurnerSyndromeCodominanceAutosomalDominantSingleNucleotidePolymorphismTranscriptionDNAMethylationGeneticAnticipationTSC-1(TuberousSclerosisGene-1)PraderWilliSyndromeRobertsonianTranslocationWilson'sDiseaseEuchromatinNF-2GenePenetranceNF1ExcessCAGRepeatsTranslocationNon-sensemutationMeioticNondisjunctionAutosomalRecessiveGWASFISHSubstitutionIntronKaryotypingKlinefelter'sSyndromeDown'sSyndromeQuantitativePCRMis-sensemutationHistoneAcetylationExonInversionmicroRNAAcuteIntermittentPorphyria

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