Patient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome.

Croonen, Ellen A

Patient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome. [electronic resource] - Clinical dysmorphology Oct 2012 - 212-214 p. digital

Publication Type: Case Reports; Journal Article

1473-5717

10.1097/MCD.0b013e3283557231 doi


Child
Child, Preschool
Diagnosis, Differential
Humans
Infant
Infant, Newborn
Mutation--genetics
Neurofibromatosis 1--genetics
Noonan Syndrome--diagnosis