Examples of using Different mutations in English and their translations into Portuguese
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and over 1500 different mutations have been determined to date.
in chromosome 12 12q22-q24, and over 500 different mutations in this locus have already been described.
The remaining 12-30% of the alleles comprise the other 2,000 different mutations, each of which, individually, have a very low frequency few mutations have a worldwide frequency above 0.1%,
this dissertation aimed to evaluate the influence of different mutations and isoforms found in the¿-amyloid peptide
enabling the concurrent identification of different mutations in several genes.
pituitary adenomas with different mutations of the gene encoding the aryl hydrocarbon receptor interacting protein aip.
We believe that there are so many different mutations that can lead to the HCM in so many different genes that it is hard to find a high number of patients with the same mutation to compare and establish the phenotype end-point with some precision.
the genetic heterogeneity more than 140 different mutations have been identified in the RPS6KA3 gene,
Have been described over 1600 different mutations in the ldlr gene associated with the phenotype of fh,
who identify four different mutations on such gene as responsible for hearing neuropathy of recessive heredity in four Spaniard families.
Three year old boy with genetically confirmed Gitelman syndrome three different mutations in SLC12A3 gene;
it can even happen to have two different mutations and make the other not appreciated normal
an individual with two different mutations in their ryanodine receptor,
Despite the large genetic variability, different mutation converge to a limited number of phenotypes.
A different mutation with a similar effect causes the chestnut colour in horses.
But it doesn't guarantee he won't develop HCM from a different mutation.
Morover, at trindade a different mutation was found in the same gene intron 10.
There were 45 different BCR-ABL mutations in 38% of patients enrolled in this study.
There were 45 different BCR-ABL mutations in 38% of patients enrolled in this trial.
Understanding the molecular basis of disease development goes beyond the identification of different causative mutations.