Wilson'sDiseaseTranscriptionExonLinkageAnalysisSilentMutationSingleNucleotidePolymorphismTranslocationIntronRobertsonianTranslocationSubstitutionMeioticNondisjunctionmicroRNAEnhancerLocusHeterogeneityNon-sensemutationPromoterInversionPraderWilliSyndromeDNAMethylationPleiotropyHistoneMethylationAutosomalDominantNF-2GeneFISHNF1Mis-sensemutationCodominancePenetranceFragile XSyndromeTSC-1(TuberousSclerosisGene-1)GWASTurnerSyndromeHeterochromatinEuchromatinKaryotypingKlinefelter'sSyndromeDown'sSyndromeAutosomalRecessiveHistoneAcetylationExcessCAGRepeatsGeneticAnticipationQuantitativePCRAcuteIntermittentPorphyriaWilson'sDiseaseTranscriptionExonLinkageAnalysisSilentMutationSingleNucleotidePolymorphismTranslocationIntronRobertsonianTranslocationSubstitutionMeioticNondisjunctionmicroRNAEnhancerLocusHeterogeneityNon-sensemutationPromoterInversionPraderWilliSyndromeDNAMethylationPleiotropyHistoneMethylationAutosomalDominantNF-2GeneFISHNF1Mis-sensemutationCodominancePenetranceFragile XSyndromeTSC-1(TuberousSclerosisGene-1)GWASTurnerSyndromeHeterochromatinEuchromatinKaryotypingKlinefelter'sSyndromeDown'sSyndromeAutosomalRecessiveHistoneAcetylationExcessCAGRepeatsGeneticAnticipationQuantitativePCRAcuteIntermittentPorphyria

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.


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