Table 1.

Analysis of individual subclones derived from paternal peripheral blood cell DNA and in vitro colonies for the presence of the 1929T>C mutation and 4890C>A polymorphism

1929T>C mutation4890C>A polymorphism
C1929 clones (colonies)/total analyzedA4890 clones/total clones analyzed
No.%No.%
Peripheral blood cells     
 CD3+ 13 of 54 24* 27 of 53 48 
 Neutrophils 6 of 84 7* 16 of 36 44  
In vitro colonies     
 BFU-E 33 of 58 57 — —  
 CFU-GM 14 of 34 41 — — 
1929T>C mutation4890C>A polymorphism
C1929 clones (colonies)/total analyzedA4890 clones/total clones analyzed
No.%No.%
Peripheral blood cells     
 CD3+ 13 of 54 24* 27 of 53 48 
 Neutrophils 6 of 84 7* 16 of 36 44  
In vitro colonies     
 BFU-E 33 of 58 57 — —  
 CFU-GM 14 of 34 41 — — 
*

Difference in the percentage of mutant clones derived from CD3+ and neutrophil DNA is statistically significant (P < .001).

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