Connection

Kenton Holden to Chromosomes, Human, X

This is a "connection" page, showing publications Kenton Holden has written about Chromosomes, Human, X.
Connection Strength

0.878
  1. Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2). J Child Neurol. 2012 Jun; 27(6):786-90.
    View in: PubMed
    Score: 0.378
  2. Autism in two females with duplications involving Xp11.22-p11.23. Dev Med Child Neurol. 2011 May; 53(5):463-6.
    View in: PubMed
    Score: 0.359
  3. Finding new etiologies of mental retardation and hypotonia: X marks the spot. Dev Med Child Neurol. 2008 Feb; 50(2):104-11.
    View in: PubMed
    Score: 0.072
  4. X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Eur J Hum Genet. 2003 Dec; 11(12):937-44.
    View in: PubMed
    Score: 0.054
  5. 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.