Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent? [electronic resource]
Producer: 20120613Description: 352-6 p. digitalISSN:- 1476-5438
- Adolescent
- Adult
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, X
- Comparative Genomic Hybridization
- Eye Proteins -- genetics
- GTP-Binding Proteins
- Gene Deletion
- Genetic Diseases, X-Linked -- complications
- Genetic Linkage
- Haplotypes
- Humans
- Infant
- Intellectual Disability -- complications
- Intracellular Signaling Peptides and Proteins -- genetics
- Kruppel-Like Transcription Factors -- genetics
- Male
- Membrane Proteins -- genetics
- Middle Aged
- Pedigree
- Retinal Dystrophies -- complications
- Syndrome
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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