TY  - GEN
AU  - Hirota,Hamao
AU  - Matsuoka,Rumiko
AU  - Chen,Xiao-Ning
AU  - Salandanan,Lora S
AU  - Lincoln,Alan
AU  - Rose,Fredric E
AU  - Sunahara,Mariko
AU  - Osawa,Makiko
AU  - Bellugi,Ursula
AU  - Korenberg,Julie R
TI  - Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23
SN  - 1098-3600
PY  - 2004///0324
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 7
KW  - Cohort Studies
KW  - Cosmids
KW  - Female
KW  - Gene Deletion
KW  - Gene Dosage
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intelligence Tests
KW  - Models, Genetic
KW  - Muscle Proteins
KW  - genetics
KW  - Nuclear Proteins
KW  - Phenotype
KW  - Physical Chromosome Mapping
KW  - Trans-Activators
KW  - Transcription Factors, TFII
KW  - Williams Syndrome
KW  - diagnosis
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1097/01.GIM.0000076975.10224.67
ER  -