His genetic deformity consists of the unique power to breathe fire.
This is, once again, due to a genetic deformity among conservatives.
One unexpected result is the differences in heritabilities between the four different fins that were observed for both fin length and fin erosion; for the first dorsal fin, estimates of heritability were extremely high for both length (0.60 to 0.80) and erosion (0.83), which may indicate the existence of a genetic deformity rather than fin damage on the first dorsal fin.
In Bub's case, the entrepreneurship is particularly unsettling because her lovability hinges on severe genetic deformities, including stunted bone growth, a misshapen jaw and a lack of teeth.
Generations of inbreeding, with no ice bridges to introduce new wolves to the island, have bred genetic deformities in the animals.
A line of 16th Century Spanish Habsburgs swimming in a limited gene pool riddled with genetic deformities and the final throes of syphilitic dementia can't hold a candle to the madness of the Cheney family.
Risk factors for recurrent miscarriage varies widely, such as maternal age, number of previous miscarriages, antiphospholipid syndrome, genetic factors, anatomical deformity of reproductive organs, endocrine disorders, immune factors, and infective agents, but in more than half of such patients, no certain diagnosis could be identified [ 4, 5].
Bishara SE et al. reported on the many and various etiologic factors that are implicated in genetic or congenital deformities (cleft lip and palate, condyle hypoplasia, hemifacial microsomia, etc)., developmental asymmetry (arising during growth), and acquired, environmental asymmetry (habits, disease, trauma, etc).
But proving that infant mortality hundreds of miles from the stricken nuclear plant has increased 20-30% in 20 years, or that the many young people suffering from genetic disorders, internal organ deformities and thyroid cancers are the victims of the world's greatest release of radioactivity, is impossible.
Non-modifiable risk factors are genetic predisposition, structural spinal deformities or disorders and female gender.
The phenotypes of Prokr2 and Prok2 knockout mice model aspects of human Kallman syndrome (KS), a partially penetrant genetic disease that causes OB deformity and consequently anosomia and hypogonadism with associated sterility and failure to reach puberty (Ng et al., 2005; Matsumoto et al., 2006).
