A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome. [electronic resource]
Producer: 20171103Description: 390-392 p. digitalISSN:- 1018-9068
- Abnormalities, Multiple
- Adolescent
- Bronchi -- abnormalities
- DiGeorge Syndrome -- complications
- Female
- Genetic Predisposition to Disease
- Humans
- Multidetector Computed Tomography
- Mutation
- Phenotype
- Predictive Value of Tests
- Pulmonary Artery -- abnormalities
- Recurrence
- Respiratory Tract Infections -- diagnosis
- Risk Factors
- T-Box Domain Proteins -- genetics
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Publication Type: Case Reports; Journal Article
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