Showing 1 - 3 results of 3 for search 'Ashley Kuhl', query time: 0.02s Refine Results
  1. 1
    Genotypes of patients with phenylalanine hydroxylase deficiency in the Wisconsin Amish

    Genotypes of patients with phenylalanine hydroxylase deficiency in the Wisconsin Amish by Jessica Scott Schwoerer, Nicoletta Drilias, Ashley Kuhl, Sean Mochal, Mei Baker

    Published 2018-06-01
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    Article
  2. 2
    Familial segregation of a 5q15‐q21.2 deletion associated with facial dysmorphism and speech delay

    Familial segregation of a 5q15‐q21.2 deletion associated with facial dysmorphism and speech delay by Cinthya Zepeda‐Mendoza, McKinsey L. Goodenberger, Ashley Kuhl, Gregory M. Rice, Nicole Hoppman

    Published 2019-06-01
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  3. 3
    No association between SCN9A and monogenic human epilepsy disorders.

    No association between SCN9A and monogenic human epilepsy disorders. by James Fasham, Joseph S Leslie, Jamie W Harrison, James Deline, Katie B Williams, Ashley Kuhl, Jessica Scott Schwoerer, Harold E Cross, Andrew H Crosby, Emma L Baple

    Published 2020-11-01
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