PraderWilliSyndromeFISHGeneticAnticipationExcessCAGRepeatsSingleNucleotidePolymorphismAcuteIntermittentPorphyriaEnhancerNF1HeterochromatinEuchromatinIntronDown'sSyndromeMeioticNondisjunctionKaryotypingLocusHeterogeneityPromoterAutosomalRecessiveLinkageAnalysisExonCodominanceInversionTSC-1(TuberousSclerosisGene-1)HistoneAcetylationQuantitativePCRKlinefelter'sSyndromeTranslocationTranscriptionTurnerSyndromePenetranceMis-sensemutationAutosomalDominantDNAMethylationSubstitutionRobertsonianTranslocationWilson'sDiseaseSilentMutationNon-sensemutationGWASPleiotropyNF-2GeneHistoneMethylationFragile XSyndromemicroRNAPraderWilliSyndromeFISHGeneticAnticipationExcessCAGRepeatsSingleNucleotidePolymorphismAcuteIntermittentPorphyriaEnhancerNF1HeterochromatinEuchromatinIntronDown'sSyndromeMeioticNondisjunctionKaryotypingLocusHeterogeneityPromoterAutosomalRecessiveLinkageAnalysisExonCodominanceInversionTSC-1(TuberousSclerosisGene-1)HistoneAcetylationQuantitativePCRKlinefelter'sSyndromeTranslocationTranscriptionTurnerSyndromePenetranceMis-sensemutationAutosomalDominantDNAMethylationSubstitutionRobertsonianTranslocationWilson'sDiseaseSilentMutationNon-sensemutationGWASPleiotropyNF-2GeneHistoneMethylationFragile XSyndromemicroRNA

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