A Novel Mutation on RAF1 in Association with Fetal Findings Suggestive of Noonan Syndrome.

Kneitel, Anna W

A Novel Mutation on RAF1 in Association with Fetal Findings Suggestive of Noonan Syndrome. [electronic resource] - Fetal and pediatric pathology 2015 - 361-4 p. digital

Publication Type: Case Reports; Journal Article

1551-3823

10.3109/15513815.2015.1087609 doi


Female
Fetus
Humans
Male
Mutation, Missense
Noonan Syndrome--genetics
Pregnancy
Prenatal Diagnosis
Proto-Oncogene Proteins c-raf--genetics