IntronDown'sSyndromeExonLocusHeterogeneityNF1AutosomalDominantSilentMutationHistoneAcetylationTurnerSyndromeSingleNucleotidePolymorphismFragile XSyndromeNF-2GenePenetranceQuantitativePCRAcuteIntermittentPorphyriaAutosomalRecessivemicroRNAPleiotropyDNAMethylationGWASKaryotypingCodominanceSubstitutionPromoterTSC-1(TuberousSclerosisGene-1)HeterochromatinEuchromatinTranscriptionEnhancerMis-sensemutationTranslocationGeneticAnticipationHistoneMethylationNon-sensemutationKlinefelter'sSyndromeRobertsonianTranslocationPraderWilliSyndromeWilson'sDiseaseInversionFISHExcessCAGRepeatsLinkageAnalysisMeioticNondisjunctionIntronDown'sSyndromeExonLocusHeterogeneityNF1AutosomalDominantSilentMutationHistoneAcetylationTurnerSyndromeSingleNucleotidePolymorphismFragile XSyndromeNF-2GenePenetranceQuantitativePCRAcuteIntermittentPorphyriaAutosomalRecessivemicroRNAPleiotropyDNAMethylationGWASKaryotypingCodominanceSubstitutionPromoterTSC-1(TuberousSclerosisGene-1)HeterochromatinEuchromatinTranscriptionEnhancerMis-sensemutationTranslocationGeneticAnticipationHistoneMethylationNon-sensemutationKlinefelter'sSyndromeRobertsonianTranslocationPraderWilliSyndromeWilson'sDiseaseInversionFISHExcessCAGRepeatsLinkageAnalysisMeioticNondisjunction

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