FEVR-like Presentation in an 11q Deletion Syndrome and 16p13.11 Microdeletion. [electronic resource]
Producer: 20171226Description: e71-e74 p. digitalISSN:- 1938-2405
- Abnormalities, Multiple
- Child
- Chromosome Deletion
- Chromosomes, Human, Pair 11 -- genetics
- DNA -- genetics
- Familial Exudative Vitreoretinopathies
- Fluorescein Angiography
- Fundus Oculi
- Humans
- Jacobsen Distal 11q Deletion Syndrome -- diagnosis
- Male
- Osteoporosis -- diagnosis
- Pedigree
- Retina -- abnormalities
- Vitreoretinopathy, Proliferative -- diagnosis
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Publication Type: Case Reports; Journal Article
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