Pontine tegmental cap dysplasia with a 2q13 microdeletion involving the NPHP1 gene: insights into malformations of the mid-hindbrain. [electronic resource]
Producer: 20100728Description: 69-74 p. digitalISSN:- 1558-0776
- Adaptor Proteins, Signal Transducing -- genetics
- Adolescent
- Brain Diseases -- complications
- Chromosome Aberrations
- Chromosome Deletion
- Cytoskeletal Proteins
- Developmental Disabilities -- complications
- Humans
- Hyperplasia -- complications
- Magnetic Resonance Imaging -- methods
- Male
- Membrane Proteins -- genetics
- Neurologic Examination
- Neurosurgery -- methods
- Pons -- abnormalities
No physical items for this record
Publication Type: Case Reports; Journal Article
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