A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia. [electronic resource]
Producer: 20151026Description: 155-7 p. digitalISSN:- 1476-5543
- Coloboma -- diagnosis
- Diagnosis
- Fatal Outcome
- Female
- Forkhead Transcription Factors -- genetics
- Humans
- Hyperplasia -- congenital
- Hypertension, Pulmonary -- diagnosis
- Infant, Newborn
- Iris -- abnormalities
- Mutation
- Persistent Fetal Circulation Syndrome -- complications
- Pulmonary Alveoli -- abnormalities
- Respiration, Artificial -- methods
- Respiratory Insufficiency -- etiology
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.