Connection

RICHARD KELLERMAYER to DNA Mutational Analysis

This is a "connection" page, showing publications RICHARD KELLERMAYER has written about DNA Mutational Analysis.
Connection Strength

0.119
  1. Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation. Pathol Oncol Res. 2005; 11(2):82-6.
    View in: PubMed
    Score: 0.053
  2. Whole-exome sequencing reveals GPIHBP1 mutations in infantile colitis with severe hypertriglyceridemia. J Pediatr Gastroenterol Nutr. 2014 Jul; 59(1):17-21.
    View in: PubMed
    Score: 0.025
  3. Presenile cataract: consider cholestanol. Arch Ophthalmol. 2006 Oct; 124(10):1490-2.
    View in: PubMed
    Score: 0.014
  4. Congenital chylothorax in Opitz G/BBB syndrome. Am J Med Genet A. 2006 May 15; 140(10):1119-21.
    View in: PubMed
    Score: 0.014
  5. Bigenic connexin mutations in a patient with hidrotic ectodermal dysplasia. Eur J Dermatol. 2005 Mar-Apr; 15(2):75-9.
    View in: PubMed
    Score: 0.013
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.