WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH. [electronic resource]
Producer: 20060727Description: 1214-8 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Blepharoptosis -- pathology
- Chromosome Banding
- Chromosome Deletion
- Chromosomes, Human, Pair 11 -- genetics
- Chromosomes, Human, Pair 15 -- genetics
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Karyotyping
- Obesity -- pathology
- Translocation, Genetic
- WAGR Syndrome -- pathology
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Publication Type: Case Reports; Journal Article
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