T. Conrad Gilliam to Genes
This is a "connection" page, showing publications T. Conrad Gilliam has written about Genes.
Connection Strength
0.363
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Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus. Neurology. 1991 Sep; 41(9):1418-22.
Score: 0.095
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A DNA segment encoding two genes very tightly linked to Huntington's disease. Science. 1987 Nov 13; 238(4829):950-2.
Score: 0.073
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Isolation of multiple genomic sequences coding for chicken myosin heavy chain protein. J Biol Chem. 1982 Jan 10; 257(1):549-56.
Score: 0.049
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Lynx: a knowledge base and an analytical workbench for integrative medicine. Nucleic Acids Res. 2016 Jan 04; 44(D1):D882-7.
Score: 0.032
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Lynx web services for annotations and systems analysis of multi-gene disorders. Nucleic Acids Res. 2014 Jul; 42(Web Server issue):W473-7.
Score: 0.029
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Lynx: a database and knowledge extraction engine for integrative medicine. Nucleic Acids Res. 2014 Jan; 42(Database issue):D1007-12.
Score: 0.028
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Chromosome jumping from D4S10 (G8) toward the Huntington disease gene. Proc Natl Acad Sci U S A. 1988 Sep; 85(17):6437-41.
Score: 0.019
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DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
Score: 0.015
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The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nat Genet. 1999 Oct; 23(2):233-6.
Score: 0.010
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Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. Am J Hum Genet. 1997 Aug; 61(2):317-28.
Score: 0.009
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The implications of genetic variation in human pathology. Biochem Soc Symp. 1984; 49:183-8.
Score: 0.004