Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

Foley, Samantha B; Rios, Jonathan J; Mgbemena, Victoria E; Robinson, Linda S; Hampel, Heather L; Toland, Amanda E; Durham, Leslie; Ross, Theodora S.

Afiliação

Foley SB; Department of Internal Medicine, UT Southwestern Medical Center, Dallas TX, 75390, USA.
Rios JJ; Sarah M. and Charles E. Seay Center for Musculoskeletal Research, Texas Scottish Rite Hospital for Children, Dallas, Texas 75219, USA ; Department of Pediatrics, McDermott Center for Human Growth and Development, and Department of Orthopaedic Surgery, UT Southwestern Medical Center, Dallas, Texas 75
Mgbemena VE; Department of Internal Medicine, UT Southwestern Medical Center, Dallas TX, 75390, USA.
Robinson LS; Department of Cancer Genetics, UT Southwestern Medical Center, Dallas, TX, 75390, USA.
Hampel HL; Department of Human Genetics, Ohio State University, Columbus, OH, 43210, USA.
Toland AE; Department of Human Genetics, Ohio State University, Columbus, OH, 43210, USA.
Durham L; Department of Internal Medicine, UT Southwestern Medical Center, Dallas TX, 75390, USA ; Sarah M. and Charles E. Seay Center for Musculoskeletal Research, Texas Scottish Rite Hospital for Children, Dallas, Texas 75219, USA.
Ross TS; Department of Internal Medicine, UT Southwestern Medical Center, Dallas TX, 75390, USA ; Department of Cancer Genetics, UT Southwestern Medical Center, Dallas, TX, 75390, USA.

EBioMedicine ; 2(1): 74-81, 2015 Jan.

Article em En | MEDLINE | ID: mdl-26023681