Kenton Holden to Intellectual Disability
This is a "connection" page, showing publications Kenton Holden has written about Intellectual Disability.
Connection Strength
0.522
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Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7.
Score: 0.267
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Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53.
Score: 0.088
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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: 0.058
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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: 0.046
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Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Pediatr Neurol. 2014 Jun; 50(6):636-9.
Score: 0.026
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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: 0.013
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Neonatal seizures. I. Correlation of prenatal and perinatal events with outcomes. Pediatrics. 1982 Aug; 70(2):165-76.
Score: 0.012
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Neurological involvement in nevus unis lateris and nevus linearis sebaceus. Neurology. 1972 Sep; 22(9):879-87.
Score: 0.006
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Neonatal seizures. II. A multivariate analysis of factors associated with outcome. Pediatrics. 1982 Aug; 70(2):177-85.
Score: 0.003
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Stopping medication in children with epilepsy: predictors of outcome. N Engl J Med. 1981 May 07; 304(19):1125-9.
Score: 0.003
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Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis. Pediatrics. 1972 Nov; 50(5):688-92.
Score: 0.001