IntronLocusHeterogeneityGWASExonAcuteIntermittentPorphyriaAutosomalDominantPleiotropyTSC-1(TuberousSclerosisGene-1)KaryotypingEuchromatinWilson'sDiseaseFragile XSyndromeRobertsonianTranslocationSingleNucleotidePolymorphismMis-sensemutationHistoneAcetylationPraderWilliSyndromeFISHHistoneMethylationAutosomalRecessiveInversionQuantitativePCRNF-2GeneLinkageAnalysismicroRNAExcessCAGRepeatsPromoterNon-sensemutationDown'sSyndromeTranslocationHeterochromatinTurnerSyndromeSubstitutionNF1GeneticAnticipationMeioticNondisjunctionPenetranceSilentMutationEnhancerTranscriptionDNAMethylationKlinefelter'sSyndromeCodominanceIntronLocusHeterogeneityGWASExonAcuteIntermittentPorphyriaAutosomalDominantPleiotropyTSC-1(TuberousSclerosisGene-1)KaryotypingEuchromatinWilson'sDiseaseFragile XSyndromeRobertsonianTranslocationSingleNucleotidePolymorphismMis-sensemutationHistoneAcetylationPraderWilliSyndromeFISHHistoneMethylationAutosomalRecessiveInversionQuantitativePCRNF-2GeneLinkageAnalysismicroRNAExcessCAGRepeatsPromoterNon-sensemutationDown'sSyndromeTranslocationHeterochromatinTurnerSyndromeSubstitutionNF1GeneticAnticipationMeioticNondisjunctionPenetranceSilentMutationEnhancerTranscriptionDNAMethylationKlinefelter'sSyndromeCodominance

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