Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?

Delphin, Nathalie

Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent? [electronic resource] - European journal of human genetics : EJHG Mar 2012 - 352-6 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1476-5438

10.1038/ejhg.2011.217 doi


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