PraderWilliSyndromeHeterochromatinSubstitutionMis-sensemutationPenetranceWilson'sDiseaseNF1KaryotypingAcuteIntermittentPorphyriaGWASMeioticNondisjunctionDown'sSyndromeExcessCAGRepeatsTurnerSyndromeFISHmicroRNAAutosomalDominantTranslocationFragile XSyndromeDNAMethylationRobertsonianTranslocationQuantitativePCRLocusHeterogeneityTranscriptionSingleNucleotidePolymorphismCodominanceNon-sensemutationEnhancerTSC-1(TuberousSclerosisGene-1)PleiotropyHistoneMethylationExonSilentMutationHistoneAcetylationKlinefelter'sSyndromeInversionGeneticAnticipationAutosomalRecessiveEuchromatinIntronPromoterLinkageAnalysisNF-2GenePraderWilliSyndromeHeterochromatinSubstitutionMis-sensemutationPenetranceWilson'sDiseaseNF1KaryotypingAcuteIntermittentPorphyriaGWASMeioticNondisjunctionDown'sSyndromeExcessCAGRepeatsTurnerSyndromeFISHmicroRNAAutosomalDominantTranslocationFragile XSyndromeDNAMethylationRobertsonianTranslocationQuantitativePCRLocusHeterogeneityTranscriptionSingleNucleotidePolymorphismCodominanceNon-sensemutationEnhancerTSC-1(TuberousSclerosisGene-1)PleiotropyHistoneMethylationExonSilentMutationHistoneAcetylationKlinefelter'sSyndromeInversionGeneticAnticipationAutosomalRecessiveEuchromatinIntronPromoterLinkageAnalysisNF-2Gene

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