Kenton Holden to Genetic Linkage
This is a "connection" page, showing publications Kenton Holden has written about Genetic Linkage.
Connection Strength
0.157
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X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Eur J Hum Genet. 2003 Dec; 11(12):937-44.
Score: 0.055
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X-linked lissencephaly with absent corpus callosum and ambiguous genitalia. Am J Med Genet. 1999 Oct 08; 86(4):331-7.
Score: 0.042
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X-linked myotubular myopathy: clinical observations in ten additional cases. Am J Med Genet. 1995 Nov 06; 59(2):168-73.
Score: 0.032
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A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family. Mol Vis. 2006 Jul 20; 12:791-5.
Score: 0.017
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X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28. Am J Hum Genet. 2002 May; 70(5):1349-56.
Score: 0.012