Kenton Holden to Pedigree
This is a "connection" page, showing publications Kenton Holden has written about Pedigree.
Connection Strength
0.317
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Transgenerational Inheritance of Familial Lipomyelomeningocele. J Child Neurol. 2017 Dec; 32(14):1118-1122.
Score: 0.146
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Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
Score: 0.076
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.022
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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 MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7.
Score: 0.016
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
Score: 0.014
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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: 0.014
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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