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
-
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.
Score: 0.378
-
Autism in two females with duplications involving Xp11.22-p11.23. Dev Med Child Neurol. 2011 May; 53(5):463-6.
Score: 0.359
-
Finding new etiologies of mental retardation and hypotonia: X marks the spot. Dev Med Child Neurol. 2008 Feb; 50(2):104-11.
Score: 0.072
-
X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Eur J Hum Genet. 2003 Dec; 11(12):937-44.
Score: 0.054
-
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.
Score: 0.015