Connection

Kenton Holden to Genetic Diseases, X-Linked

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This is a "connection" page, showing publications Kenton Holden has written about Genetic Diseases, X-Linked.
Kenton Holden
Connection Strength
0.180
Genetic Diseases, X-Linked
  1. ?-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. Brain. 2013 Jun; 136(Pt 6):1708-17.
    View in: PubMed
    Score: 0.104
  2. X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7.
    View in: PubMed
    Score: 0.061
  3. A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. Am J Med Genet A. 2005 Sep 15; 138(1):70-2.
    View in: PubMed
    Score: 0.015
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.