Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.
Hirota, Hamao
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. [electronic resource] - Genetics in medicine : official journal of the American College of Medical Genetics - 311-21 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1098-3600
10.1097/01.GIM.0000076975.10224.67 doi
Adolescent
Adult
Child
Chromosome Mapping
Chromosomes, Human, Pair 7
Cohort Studies
Cosmids
Female
Gene Deletion
Gene Dosage
Humans
In Situ Hybridization, Fluorescence
Intelligence Tests
Models, Genetic
Muscle Proteins--genetics
Nuclear Proteins--genetics
Phenotype
Physical Chromosome Mapping
Trans-Activators--genetics
Transcription Factors, TFII--genetics
Williams Syndrome--diagnosis
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. [electronic resource] - Genetics in medicine : official journal of the American College of Medical Genetics - 311-21 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1098-3600
10.1097/01.GIM.0000076975.10224.67 doi
Adolescent
Adult
Child
Chromosome Mapping
Chromosomes, Human, Pair 7
Cohort Studies
Cosmids
Female
Gene Deletion
Gene Dosage
Humans
In Situ Hybridization, Fluorescence
Intelligence Tests
Models, Genetic
Muscle Proteins--genetics
Nuclear Proteins--genetics
Phenotype
Physical Chromosome Mapping
Trans-Activators--genetics
Transcription Factors, TFII--genetics
Williams Syndrome--diagnosis