The phrase "a consanguinity" is correct and usable in written English.
It can be used when referring to a relationship or connection by blood, often in discussions about genetics, family ties, or legal matters.
Example: "The consanguinity between the two individuals was established through a detailed genealogical study."
Alternatives: "a blood relationship" or "a familial connection".
Interestingly, every family sequenced thus far has a different underlying putative defective gene(s) precluding our ability to provide supporting evidence for the hypothesis that suggests the presence of a consanguinity-driven common genetic haplotype associated with increased susceptibility to breast cancer [ 98].
He could have taken for granted a certain consanguinity in the area and moved on to point out that the Tasaday are not only ineluctably involved with the local social and political scene, but also with international questions of justice which make it impermissible for "lost" tribes to remain either idealised or artificially sequestered.
In summary, a molecular genetic diagnosis can be reached in ~75% of patients with diabetes onset ≤6 months of age when KCNJ11, INS and ABCC8 genes are sequenced in populations with a low consanguinity rate.
Meanwhile, the prejudice of low levels of HDL cholesterol in cardiovascular system became increasingly prominent, which had a tight consanguinity with myocardial infarction and death from coronary heart disease (CHD).
A major concern is avoiding consanguinity, a fancy word for the socially taboo and possibly genetically disastrous mating of blood relatives.
While analyzing the risk factors associated with blindness in these children, we found that blindness was more prevalent in the Terai region, in the female population in children of older age group, with a history of consanguinity and with an illiterate mother.
In summary, we have demonstrated that during the genetics evaluation of an individual affected by a rare disorder in the setting of consanguinity, a SNP array analysis should be considered, unless the diagnosis is obvious.
Finally, having used the approach as outlined above without arriving at a diagnosis against a background of consanguinity, such negative finding adds to the suspicion that the disorder may not have been documented before or, more likely, that the causative locus has not yet been mapped.
New York State utilizes a table of consanguinity that prescribes the heirs at law when a decedent died without a Last Will and Testament.
Our findings suggest that when an autosomal recessive ataxia is suspected, a single exome will provide a genetic diagnosis at least 30% of the time in a known disease gene and that this diagnostic rate will increase to ∼50% if there is an affected sibling or a history of consanguinity.
