Author/Creator: Powell‐Hamilton, Nina - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Powell‐Hamilton, Nina

1. A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair. Issue 9 (5th June 2016)

Authors:: Gripp, Karen W.; Aldinger, Kimberly A.; Bennett, James T.; Baker, Laura; Tusi, Jessica; Powell‐Hamilton, Nina; Stabley, Deborah; Sol‐Church, Katia; Timms, Andrew E.; Dobyns, William B.
Journal:: American journal of medical genetics
Issue:: Volume 170:Issue 9(2016)
Page Start:: 2237
Record Type:: Journal Article
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2. Inherited intragenic PBX1 deletion: Expanding the phenotype. Issue 1 (24th October 2020)

Authors:: Fitzgerald, Kristi K.; Powell‐Hamilton, Nina; Shillingford, Amanda J.; Robinson, Bradley; Gripp, Karen W.
Journal:: American journal of medical genetics
Issue:: Volume 185:Issue 1(2021)
Page Start:: 234
Record Type:: Journal Article
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