Somatic PIK3CA mutations in seven patients with PIK3CA-related overgrowth spectrum. [electronic resource]
Producer: 20171030Description: 978-984 p. digitalISSN:- 1552-4833
- Adolescent
- Child
- Child, Preschool
- Class I Phosphatidylinositol 3-Kinases -- genetics
- Female
- Gene Expression
- Genetic Association Studies
- Genetic Testing
- Humans
- Klippel-Trenaunay-Weber Syndrome -- diagnosis
- Male
- Mutation
- Nevus -- diagnosis
- Phenotype
- Polymerase Chain Reaction -- methods
- Scoliosis -- diagnosis
- Vascular Malformations -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.