QuantitativePCRPenetranceGeneticAnticipationFragile XSyndromeLinkageAnalysisEnhancerMis-sensemutationAcuteIntermittentPorphyriaTranslocationHistoneAcetylationSilentMutationKaryotypingExonPromoterGWASHistoneMethylationSubstitutionKlinefelter'sSyndromeDNAMethylationInversionSingleNucleotidePolymorphismIntronFISHEuchromatinHeterochromatinNF-2GeneTurnerSyndromeAutosomalRecessiveDown'sSyndromeTranscriptionExcessCAGRepeatsPleiotropymicroRNANon-sensemutationLocusHeterogeneityCodominanceNF1PraderWilliSyndromeWilson'sDiseaseAutosomalDominantMeioticNondisjunctionRobertsonianTranslocationTSC-1(TuberousSclerosisGene-1)QuantitativePCRPenetranceGeneticAnticipationFragile XSyndromeLinkageAnalysisEnhancerMis-sensemutationAcuteIntermittentPorphyriaTranslocationHistoneAcetylationSilentMutationKaryotypingExonPromoterGWASHistoneMethylationSubstitutionKlinefelter'sSyndromeDNAMethylationInversionSingleNucleotidePolymorphismIntronFISHEuchromatinHeterochromatinNF-2GeneTurnerSyndromeAutosomalRecessiveDown'sSyndromeTranscriptionExcessCAGRepeatsPleiotropymicroRNANon-sensemutationLocusHeterogeneityCodominanceNF1PraderWilliSyndromeWilson'sDiseaseAutosomalDominantMeioticNondisjunctionRobertsonianTranslocationTSC-1(TuberousSclerosisGene-1)

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