Hasil Pencarian - Lisa G Shaffer

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  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. oleh Jill A Rosenfeld, Blake C Ballif, Ann Lucas, Edward J Spence, Cynthia Powell, Arthur S Aylsworth, Beth A Torchia, Lisa G Shaffer

    Diterbitkan 2009-08-01
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  2. 2
    Large inverted duplications in the human genome form via a fold-back mechanism.

    Large inverted duplications in the human genome form via a fold-back mechanism. oleh Karen E Hermetz, Scott Newman, Karen N Conneely, Christa L Martin, Blake C Ballif, Lisa G Shaffer, Jannine D Cody, M Katharine Rudd

    Diterbitkan 2014-01-01
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  3. 3
    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. oleh 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

    Diterbitkan 2010-08-01
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