Showing 1 - 2 results of 2 for search 'Beth S Torchia', query time: 0.03s Refine Results
  1. 1
    Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.

    Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome. by Jill A Rosenfeld, Blake C Ballif, Ann Lucas, Edward J Spence, Cynthia Powell, Arthur S Aylsworth, Beth A Torchia, Lisa G Shaffer

    Published 2009-08-01
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    Article
  2. 2
    A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33.

    A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33. by Ryan N Traylor, Damien L Bruno, Trent Burgess, Robert Wildin, Anne Spencer, Devika Ganesamoorthy, David J Amor, Matthew Hunter, Matthew Hunter, Michael Caplan, Jill A Rosenfeld, Aaron Theisen, Beth S Torchia, Lisa G Shaffer, Blake C Ballif, Howard R Slater

    Published 2010-08-01
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    Article

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