TY  - GEN
AU  - Yamamoto,Toshiyuki
AU  - Mencarelli,Maria Antonietta
AU  - Di Marco,Chiara
AU  - Mucciolo,Mafalda
AU  - Vascotto,Marina
AU  - Balestri,Paolo
AU  - Gérard,Marion
AU  - Mathieu-Dramard,Michèle
AU  - Andrieux,Joris
AU  - Breuning,Martijn
AU  - Hoffer,Mariëtte J V
AU  - Ruivenkamp,Claudia A L
AU  - Shimada,Shino
AU  - Sangu,Noriko
AU  - Shimojima,Keiko
AU  - Umezu,Ryoji
AU  - Kawame,Hiroshi
AU  - Matsuo,Mari
AU  - Saito,Kayoko
AU  - Renieri,Alessandra
AU  - Mari,Francesca
TI  - Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA
SN  - 1878-0849
PY  - 2014///1215
KW  - Adolescent
KW  - Child, Preschool
KW  - Chromosome Banding
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 15
KW  - genetics
KW  - DNA Copy Number Variations
KW  - Female
KW  - Genetic Association Studies
KW  - methods
KW  - Genotype
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - Male
KW  - Nuclear Proteins
KW  - Nuclear Receptor Subfamily 1, Group F, Member 1
KW  - Phenotype
KW  - Transcriptional Elongation Factors
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ejmg.2014.02.001
ER  -