Microdeletion found by array-CGH in girl with blepharophimosis syndrome and apparently balanced translocation t(3;15)(q23;q25). [electronic resource]
Producer: 20120926Description: 107-10 p. digitalISSN:- 1744-5094
- Blepharophimosis -- genetics
- Blepharoptosis -- genetics
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 15 -- genetics
- Chromosomes, Human, Pair 3 -- genetics
- Comparative Genomic Hybridization
- DNA Mutational Analysis
- Female
- Forkhead Box Protein L2
- Forkhead Transcription Factors -- genetics
- Humans
- Karyotype
- RNA, Long Noncoding
- RNA, Untranslated -- genetics
- Translocation, Genetic
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.