Back to Results
First PageMeta Content
Syndromes / Chromosomes / Cytogenetics / Medical genetics / Agenesis of the corpus callosum / 1p36 deletion syndrome / Corpus callosum / WAGR syndrome / DiGeorge syndrome / Genetics / Biology / Health


RESEARCH ARTICLE Identification of Genomic Loci Contributing to Agenesis of the Corpus Callosum Mary C. O’Driscoll,1* Graeme C. M. Black,1 Jill Clayton-Smith,1 Elliott H. Sherr,2 and William B. Dobyns3 1
Add to Reading List

Document Date: 2013-03-05 20:09:51

Open Document

File Size: 313,55 KB

Share Result on Facebook

City

Bassi / Chiu / Walsh / San Francisco / Williams / Molina / Mencarelli / Manchester / Park / Telfer / Petersen / Krantz / Battaglia / Spinner / Katznelson / Barrett / Wing / Bonati / Desai / /

Company

Gould / Central Manchester Foundation Trust / Ó 2010 Wiley-Liss Inc. / Bhide AG / France HF / Farrell SA / Schell-Apacik Ó 2010 Wiley-Liss Inc. / Brown SA / Chudley AE / Bhalerao SA. / LG / Reekers AB / Delmonaco AG / Case / Ensembl Resources / /

Continent

Europe / /

Country

United Kingdom / /

Currency

pence / /

/

Facility

University of Manchester / Masada / Wiley Online Library / University of California-San Francisco / St Mary’s Hospital / Cryptic terminal / University of Chicago / /

IndustryTerm

appropriate online databases / brain imaging figures / magnetic resonance imaging / online version / brain imaging abnormalities / online databases / imaging / molecular and cytogenetic technology / brain imaging studies / brain imaging / online searchable database / mid-sagittal magnetic resonance imaging / Online Library / search engine / /

MedicalCondition

microcephaly / lissencephaly / hydrocephalus / Beckwith-Wiedemann syndrome / Retinoblastoma / seizures / cysts / Wilms tumor / Jacobsen syndrome / metabolic disorders / Klinefelter syndrome / callosal disorder / birth defects / Factor VII deficiency / mental retardation / nervous system anomalies / WAGR syndrome / diseases / polymicrogyria / epilepsy / cortical malformation polymicrogyria / specific developmental disabilities / disorders / Down syndrome / neural tube defects / holoprosencephaly / trisomy 21 / MS / Rett syndrome / congenital heart defects / periventricular nodular heterotopia / Andermann syndrome / imperforate anus / Polymicrogyria Locus 1p36 / polydactyly / nervous system malformations / syndrome / genetic disorders / /

MusicGroup

FISH / /

Organization

Dimes Foundation / Santos AC / Santos SR / California Department of Public Health / University of Manchester / National Institute of Health / Manchester Academic Health Sciences Centre / University of Chicago / Chicago / California Department of Human Genetics / NIHR/Manchester Biomedical Research Centre / Department of Neurology / St Mary’s Hospital / University of California-San Francisco / San Francisco / /

Person

Marcus Gunn / Lopez Pajares / Van Roy / Mary King / Ann Hum Genet / H. Sherr / Van den Neucker / Kathy Millen / Van Dael / Van Regemorter / Santos SR / Ann Genet / /

Position

Dobyns WB / Major / HB / Walker / WB / reporting physician / WB / Black GC / Hunter / King for organizational support / /

Product

Koss P15 Headphone/Headset / FS / /

ProvinceOrState

New Brunswick / Alabama / Alaska / Connecticut / Montana / Mississippi / California / Illinois / South Dakota / Manitoba / North Carolina / Massachusetts / /

Technology

gene mapping / human genome / jsp / molecular and cytogenetic technology / magnetic resonance imaging / DNA Chip / genotype / recombination / tomography / hybridization / ultrasound / search engine / MRI / artificial intelligence / /

URL

http /

SocialTag