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