ExcessCAGRepeatsTurnerSyndromeCodominancePromoterTSC-1(TuberousSclerosisGene-1)AcuteIntermittentPorphyriaPleiotropyAutosomalRecessivePraderWilliSyndromeFISHGeneticAnticipationMis-sensemutationEuchromatinLinkageAnalysisAutosomalDominantTranslocationHistoneAcetylationTranscriptionNF-2GeneLocusHeterogeneityInversionHistoneMethylationQuantitativePCRSubstitutionRobertsonianTranslocationExonHeterochromatinPenetranceNF1GWASSingleNucleotidePolymorphismKaryotypingMeioticNondisjunctionFragile XSyndromemicroRNAEnhancerNon-sensemutationIntronWilson'sDiseaseDNAMethylationKlinefelter'sSyndromeSilentMutationDown'sSyndromeExcessCAGRepeatsTurnerSyndromeCodominancePromoterTSC-1(TuberousSclerosisGene-1)AcuteIntermittentPorphyriaPleiotropyAutosomalRecessivePraderWilliSyndromeFISHGeneticAnticipationMis-sensemutationEuchromatinLinkageAnalysisAutosomalDominantTranslocationHistoneAcetylationTranscriptionNF-2GeneLocusHeterogeneityInversionHistoneMethylationQuantitativePCRSubstitutionRobertsonianTranslocationExonHeterochromatinPenetranceNF1GWASSingleNucleotidePolymorphismKaryotypingMeioticNondisjunctionFragile XSyndromemicroRNAEnhancerNon-sensemutationIntronWilson'sDiseaseDNAMethylationKlinefelter'sSyndromeSilentMutationDown'sSyndrome

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