Typical renal-coloboma syndrome phenotype in a patient with a submicroscopic deletion of the PAX2 gene. [electronic resource]
Producer: 20120924Description: 1437-41 p. digitalISSN:- 1552-4833
- Adolescent
- Biopsy
- Child
- Child, Preschool
- Coloboma -- diagnosis
- Glomerulosclerosis, Focal Segmental -- pathology
- Humans
- Infant
- Kidney -- diagnostic imaging
- PAX2 Transcription Factor -- genetics
- Phenotype
- Renal Insufficiency -- diagnosis
- Sequence Deletion
- Ultrasonography
- Vesico-Ureteral Reflux -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.