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Connection

Darrel J. Waggoner to In Situ Hybridization, Fluorescence

This is a "connection" page, showing publications Darrel J. Waggoner has written about In Situ Hybridization, Fluorescence.
  1. Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13. Am J Med Genet A. 2008 Jun 01; 146A(11):1414-22.
    View in: PubMed
    Score: 0.072
  2. Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome. Am J Med Genet A. 2007 May 15; 143A(10):1082-6.
    View in: PubMed
    Score: 0.067
  3. Deletion of 1q in a patient with acrofacial dysostosis. Am J Med Genet. 1999 Feb 12; 82(4):301-4.
    View in: PubMed
    Score: 0.038
  4. Calibration of 6q subtelomere deletions to define genotype/phenotype correlations. Clin Genet. 2005 May; 67(5):396-403.
    View in: PubMed
    Score: 0.014
  5. Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase. Mamm Genome. 2000 May; 11(5):409-11.
    View in: PubMed
    Score: 0.010
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.