AcuteIntermittentPorphyriaInversionLocusHeterogeneitySilentMutationTranslocationKaryotypingCodominanceSingleNucleotidePolymorphismTurnerSyndromeTSC-1(TuberousSclerosisGene-1)PromoterRobertsonianTranslocationAutosomalRecessiveKlinefelter'sSyndromeEnhancerWilson'sDiseaseAutosomalDominantLinkageAnalysisMis-sensemutationIntronEuchromatinPleiotropyHistoneMethylationGWASMeioticNondisjunctionHistoneAcetylationExonDNAMethylationNF-2GeneGeneticAnticipationExcessCAGRepeatsNF1Non-sensemutationSubstitutionmicroRNAHeterochromatinPenetranceTranscriptionFragile XSyndromeQuantitativePCRFISHPraderWilliSyndromeDown'sSyndromeAcuteIntermittentPorphyriaInversionLocusHeterogeneitySilentMutationTranslocationKaryotypingCodominanceSingleNucleotidePolymorphismTurnerSyndromeTSC-1(TuberousSclerosisGene-1)PromoterRobertsonianTranslocationAutosomalRecessiveKlinefelter'sSyndromeEnhancerWilson'sDiseaseAutosomalDominantLinkageAnalysisMis-sensemutationIntronEuchromatinPleiotropyHistoneMethylationGWASMeioticNondisjunctionHistoneAcetylationExonDNAMethylationNF-2GeneGeneticAnticipationExcessCAGRepeatsNF1Non-sensemutationSubstitutionmicroRNAHeterochromatinPenetranceTranscriptionFragile XSyndromeQuantitativePCRFISHPraderWilliSyndromeDown'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.


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