Table 2.
Incidence of anomalies caused by TCDD in fetuses from heterozygous hAHR parents
Genotype of fetuses | TCDD dose, μg/kg | Dams examined, n | Fetuses examined, n | Fetuses with
|
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---|---|---|---|---|---|---|---|---|
Cleft palate
|
Hydronephrosis
|
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n | %* | n | %* | Severity: 0–3.0 | ||||
Ahrb-1/b-1 | 40 | 9 | 9 | 100 | 9 | 100.0 | 2.47 ± 0.14† | |
Hetero-hAHR | 40 | 7 | 25 | 12 | 48 | 22 | 88.0 | 2.46 ± 0.13 |
Homo-hAHR | 40 | 12 | 0 | 0 | 8 | 66.6 | 1.17 ± 0.01† |
Percentage of fetuses with each anomaly out of all fetuses examined.
Significant difference between homozygous hAHR and Ahrb-1/b-1 fetuses (P < 0.0001).