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Holden, Kenton
One or more keywords matched the following items that are connected to
Holden, Kenton
Item Type
Name
Academic Article
X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome.
Academic Article
A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.
Academic Article
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
Academic Article
X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.
Academic Article
POMGnT1 gene alterations in a family with neurological abnormalities.
Academic Article
X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype.
Academic Article
Natural history of Christianson syndrome.
Concept
Pedigree
Academic Article
Transgenerational Inheritance of Familial Lipomyelomeningocele.
Search Criteria
Pedigree