Center-Authored Papers

Filters: Author is Leppig, Kathleen A  [Clear All Filters]
2011
Click ES, Cox B, Olson SB, Grompe M, Akkari Y, Moreau LA, Shimamura A, Sternen DL, Liu YJ, Leppig KA et al..  2011.  Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene.. American journal of medical genetics. Part A. 155A(7):1673-9. Abstract
2012
Fullerton SM, Wolf WA, Brothers KB, Clayton EW, Crawford DC, Denny JC, Greenland P, Koenig BA, Leppig KA, Lindor NM et al..  2012.  Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.. Genetics in medicine : official journal of the American College of Medical Genetics. Abstract
2015
Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS et al..  2015.  Actionable exomic incidental findings in 6503 participants: challenges of variant classification.. Genome research. 25(3):305-15. Abstract