Only two orthologous counterparts were recovered from C. lividus and C. sanguinolentus (livi_2 and sang_1; livi_11, livi_11 and sang 3; Figure 2; Table 2), even though these two species diverged less than 0.3 million years ago and may actually represent genetically differentiated populations of C. sanguinolentus[ 19, 49].
It can therefore be speculated that the "inert or deficient local biology" at the fracture site seen in these cases may represent a genetically predisposed environment with reduced potentials for bone regeneration.
Using data from a population genealogy of Utah record linked to a statewide cancer registry, we identified a subset of CRC cases that exhibited familial clustering in excess of that expected for all CRC cases in general, which may represent a genetically homogeneous subset of CRC.
Population declines became pronounced as early as the mid-1700s and included overall reductions in abundance (Hall et al. 2012) as well as the loss of unique spawning forms (or morphs) that may have represented genetically distinct subpopulations (Chapman 1884).
There is thus little chance the various stems at Jurupa represent genetically different individuals.
Moreover, some studies have shown that ORF5 and the non-structural protein 2 (NSP2 -coding geNSP2 -codingy represent the most genetically variable regionsp2n PRRSV genomay [16], [18], [22]–[25].
28 Some suggest that the comorbidity of PTSD with substance abuse may represent a shared genetically mediated vulnerability to psychopathology after trauma exposure.
Furthermore, these data represent statistics resulting from a single pairing of mtDNA types, and it is thus arguable how conclusions drawn from them may represent the more genetically diverse reality of biology.
This subset of CRC cases may represent a more genetically homogeneous endotype of CRC; a study focus on these cases and pedigrees may be more statistically powerful for genetic mapping because of enhanced phenotype refinement.
Autism spectrum disorder families with IQ ≥ 70 may represent a more genetically homogenous group, while the families that have rare single gene disorders, undetected chromosomal abnormalities, or de novo copy number variations tend as a whole to have lower IQ (66) and including them in a linkage analysis may reduce power.
