PraderWilliSyndromeTranslocationmicroRNAMis-sensemutationSubstitutionPleiotropyEnhancerAcuteIntermittentPorphyriaInversionFragile XSyndromeTurnerSyndromeSilentMutationHeterochromatinFISHGWASTSC-1(TuberousSclerosisGene-1)AutosomalDominantKlinefelter'sSyndromeGeneticAnticipationNF1PenetranceIntronEuchromatinHistoneAcetylationSingleNucleotidePolymorphismMeioticNondisjunctionWilson'sDiseaseCodominanceNF-2GeneLocusHeterogeneityTranscriptionAutosomalRecessiveNon-sensemutationDown'sSyndromePromoterExcessCAGRepeatsExonRobertsonianTranslocationKaryotypingQuantitativePCRDNAMethylationLinkageAnalysisHistoneMethylationPraderWilliSyndromeTranslocationmicroRNAMis-sensemutationSubstitutionPleiotropyEnhancerAcuteIntermittentPorphyriaInversionFragile XSyndromeTurnerSyndromeSilentMutationHeterochromatinFISHGWASTSC-1(TuberousSclerosisGene-1)AutosomalDominantKlinefelter'sSyndromeGeneticAnticipationNF1PenetranceIntronEuchromatinHistoneAcetylationSingleNucleotidePolymorphismMeioticNondisjunctionWilson'sDiseaseCodominanceNF-2GeneLocusHeterogeneityTranscriptionAutosomalRecessiveNon-sensemutationDown'sSyndromePromoterExcessCAGRepeatsExonRobertsonianTranslocationKaryotypingQuantitativePCRDNAMethylationLinkageAnalysisHistoneMethylation

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