PraderWilliSyndromeKaryotypingCodominanceWilson'sDiseaseInversionMis-sensemutationDNAMethylationEuchromatinHeterochromatinHistoneMethylationLocusHeterogeneityEnhancerTSC-1(TuberousSclerosisGene-1)microRNANon-sensemutationAutosomalDominantMeioticNondisjunctionExcessCAGRepeatsTranslocationAcuteIntermittentPorphyriaPenetranceTurnerSyndromeKlinefelter'sSyndromeHistoneAcetylationQuantitativePCRPleiotropyFragile XSyndromeNF1SingleNucleotidePolymorphismExonLinkageAnalysisSubstitutionGWASPromoterDown'sSyndromeIntronSilentMutationTranscriptionNF-2GeneFISHRobertsonianTranslocationAutosomalRecessiveGeneticAnticipationPraderWilliSyndromeKaryotypingCodominanceWilson'sDiseaseInversionMis-sensemutationDNAMethylationEuchromatinHeterochromatinHistoneMethylationLocusHeterogeneityEnhancerTSC-1(TuberousSclerosisGene-1)microRNANon-sensemutationAutosomalDominantMeioticNondisjunctionExcessCAGRepeatsTranslocationAcuteIntermittentPorphyriaPenetranceTurnerSyndromeKlinefelter'sSyndromeHistoneAcetylationQuantitativePCRPleiotropyFragile XSyndromeNF1SingleNucleotidePolymorphismExonLinkageAnalysisSubstitutionGWASPromoterDown'sSyndromeIntronSilentMutationTranscriptionNF-2GeneFISHRobertsonianTranslocationAutosomalRecessiveGeneticAnticipation

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