Mutations in STK11 identified exclusively in individuals with clinical histories suggestive of Peutz-Jeghers syndrome

• Authors: J.S. Dolinsky; S.B. Keiles; T.F. Pesaran; C. Horton; M. Umali; K. McGoldrick; S. Li; E. Chao
• Collaborators: University of California, Irvine
• Conference: ASHG 2014
• Date: Saturday, Oct 18, 2014 12:00am - 12:00pm