AutosomalDominantFragile XSyndromeAutosomalRecessiveGWASMis-sensemutationInversionTranscriptionLinkageAnalysisNon-sensemutationEnhancerTSC-1(TuberousSclerosisGene-1)HeterochromatinPenetranceCodominancePleiotropyWilson'sDiseaseRobertsonianTranslocationExonGeneticAnticipationSubstitutionAcuteIntermittentPorphyriaKaryotypingLocusHeterogeneityTurnerSyndromePromoterSilentMutationIntronDown'sSyndromeHistoneAcetylationDNAMethylationFISHMeioticNondisjunctionHistoneMethylationNF-2GeneQuantitativePCRPraderWilliSyndromeEuchromatinSingleNucleotidePolymorphismTranslocationKlinefelter'sSyndromeExcessCAGRepeatsNF1microRNAAutosomalDominantFragile XSyndromeAutosomalRecessiveGWASMis-sensemutationInversionTranscriptionLinkageAnalysisNon-sensemutationEnhancerTSC-1(TuberousSclerosisGene-1)HeterochromatinPenetranceCodominancePleiotropyWilson'sDiseaseRobertsonianTranslocationExonGeneticAnticipationSubstitutionAcuteIntermittentPorphyriaKaryotypingLocusHeterogeneityTurnerSyndromePromoterSilentMutationIntronDown'sSyndromeHistoneAcetylationDNAMethylationFISHMeioticNondisjunctionHistoneMethylationNF-2GeneQuantitativePCRPraderWilliSyndromeEuchromatinSingleNucleotidePolymorphismTranslocationKlinefelter'sSyndromeExcessCAGRepeatsNF1microRNA

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