Connection

SANDRA DARILEK to Base Sequence

This is a "connection" page, showing publications SANDRA DARILEK has written about Base Sequence.
Connection Strength

0.049
  1. DNA sequence analysis and genotype-phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy. BMJ Open. 2015 May 19; 5(5):e007506.
    View in: PubMed
    Score: 0.022
  2. Infrequency of two deletion mutations at the DFNB1 locus in patients and controls. Am J Med Genet A. 2008 Apr 01; 146A(7):934-6.
    View in: PubMed
    Score: 0.014
  3. DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls. Am J Med Genet A. 2006 Nov 15; 140(22):2401-15.
    View in: PubMed
    Score: 0.012
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.