TY  - GEN
AU  - Delphin,Nathalie
AU  - Hanein,Sylvain
AU  - Taie,Lucas Fares
AU  - Zanlonghi,Xavier
AU  - Bonneau,Dominique
AU  - Moisan,Jean-Paul
AU  - Boyle,Christine
AU  - Nitschke,Patrick
AU  - Pruvost,Solenn
AU  - Bonnefont,Jean-Paul
AU  - Munnich,Arnold
AU  - Roche,Olivier
AU  - Kaplan,Josseline
AU  - Rozet,Jean-Michel
TI  - Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?
SN  - 1476-5438
PY  - 2012///0613
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, X
KW  - Comparative Genomic Hybridization
KW  - Eye Proteins
KW  - genetics
KW  - GTP-Binding Proteins
KW  - Gene Deletion
KW  - Genetic Diseases, X-Linked
KW  - complications
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Intracellular Signaling Peptides and Proteins
KW  - Kruppel-Like Transcription Factors
KW  - Male
KW  - Membrane Proteins
KW  - Middle Aged
KW  - Pedigree
KW  - Retinal Dystrophies
KW  - Syndrome
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ejhg.2011.217
ER  -