Kenton Holden to Sequence Deletion
This is a "connection" page, showing publications Kenton Holden has written about Sequence Deletion.
Connection Strength
0.770
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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: 0.385
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A novel mutation in type II methemoglobinemia. J Child Neurol. 2010 Jan; 25(1):91-3.
Score: 0.322
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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: 0.062