22q11 - Robuta Search

https://scholars.duke.edu/publication/1063474 Scholars@Duke publication: Social cognitive training in adolescents with chromosome 22q11.2... cognitive training https://www.wikidata.org/wiki/Q52901694 High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions. -... scientific article published in May 1998 https://tobias-lib.uni-tuebingen.de/xmlui/handle/10900/115429 First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free... https://scholars.duke.edu/publication/797872 Scholars@Duke publication: Chromosome 22q11.2 deletion syndrome in African-American patients: a... https://scholars.duke.edu/publication/838101 Scholars@Duke publication: Assessment of parental disclosure of a 22q11.2 deletion syndrome... https://scholars.duke.edu/grant/171061 Scholars@Duke grant: Neural correlates of working memory in children with 22q11.2 deletion syndrome https://scholars.duke.edu/publication/1096951 Scholars@Duke publication: Velocardiofacial syndrome (Chromosome 22q11.2 deletion syndrome) as a... scholars duke publication syndrome https://scholars.duke.edu/publication/1105253 Scholars@Duke publication: Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot... https://childnervoussystem.blogspot.com/2017/04/a-22q112-potpourri.html pediatric neurology: A 22q11.2 potpourri Wither RG, Borlot F, MacDonald A, Butcher NJ, Chow EWC, Bassett AS, Andrade DM. 22q11.2 deletion syndrome lowers seizure threshold in adult... pediatric neurology potpourri https://scholars.duke.edu/publication/912171 Scholars@Duke publication: Vasomotor instability in chromosome 22q11 deletion. scholars duke publication instability chromosome https://pubmed.ncbi.nlm.nih.gov/35033576/ Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome Noninvasive cell-free DNA prenatal screening for 22q11.2 deletion syndrome can detect most affected cases, including smaller nested deletions, with a low false... cell free dna https://scholars.duke.edu/publication/1024326 Scholars@Duke publication: Psychiatric disorders from childhood to adulthood in 22q11.2 deletion... https://open.library.emory.edu/concern/publications/01f936cf-17f2-47ba-a7da-9f2ea0bbd035 Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a... Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a multilevel approach to defining core disease processes https://cordis.europa.eu/project/id/GENE930053 Hemizygosity of chromosome 22q11 and human birth defects | Project | Fact Sheet | FP3-BIOMED 1 |... Hemizygosity for a region of chromosome 22q11 causes a wide range of congenital defects including Digeorge syndrome, Shprintzen (velo-cardiofacial syndrome)... https://pubmed.ncbi.nlm.nih.gov/29141125/ Elevated Proinflammatory Markers in 22q11.2 Deletion Syndrome Are Associated With Psychosis and... Our preliminary findings indicate an involvement of inflammatory processes in the pathophysiology of psychosis and cognitive deficits in 22q11.2DS and are in... https://give.ucdavis.edu/MIND/22Q11DE?appeal=21544 Give UC Davis - Chromosome 22q11.2 Deletion Syndrome Research Donate to the University of California at Davis uc davis give chromosome deletion syndrome https://kidshealth.org/ChildrensHealthNetwork/en/parents/22q11-deletion.html 22q11.2 Deletion Syndrome (DiGeorge Syndrome) (for Parents) - Children's Health Network 22q11.2 deletion syndrome (also called DiGeorge Syndrome) is a genetic condition that can cause a variety of physical and behavioral problems. for parents deletion syndrome https://scholars.duke.edu/publication/731368 Scholars@Duke publication: Reactive lymphoid hyperplasia in association with 22q11.2 deletion... in association with https://give.ucdavis.edu/MIND/22Q11DE?appeal=22151 Give UC Davis - Chromosome 22q11.2 Deletion Syndrome Research Donate to the University of California at Davis uc davis give chromosome deletion syndrome https://give.ucdavis.edu/MIND/22Q11DE?appeal=22A81 Give UC Davis - Chromosome 22q11.2 Deletion Syndrome Research Donate to the University of California at Davis uc davis give chromosome deletion syndrome https://pubmed.ncbi.nlm.nih.gov/23765047/ Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome The results suggest that neonatal seizures may increase the risk for more severe intellectual deficits in 22q11.2 deletion syndrome, likely mediated by... intellectual disability neonatal hypocalcemia seizures https://scholars.duke.edu/publication/1424419 Scholars@Duke publication: Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2... https://research.manchester.ac.uk/en/publications/chromosome-22q11-deletions-are-not-found-in-autistic-patients-ide/ Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic... https://openresearch.surrey.ac.uk/esploro/outputs/journalArticle/Epilepsy-and-seizures-in-young-people/99783502202346 Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with... The true prevalence of epileptic seizures and epilepsy in 22q11.2 deletion syndrome (22q11.2DS) is unknown, because previous studies have relied on historical... epilepsy and seizures https://www.22q11.pl/ Stowarzyszenie 22q11 Polska - Stowarzyszenie 22q11 Polska Jun 24, 2026 - Jeśli 22q11 pojawiło się w Twoim życiu – prywatnie lub zawodowo – trafiłeś w dobre miejsce! Stowarzyszenie 22q11 Polska powstało z inicjatywy rodziców dzieci z… stowarzyszenie polska https://eprints.ncl.ac.uk/233047 Positive and Negative Experiences of Parenting a Pre-school Child with 22q11.2 Deletion Syndrome -... https://bs.wikipedia.org/wiki/Sindrom_distalne_delecije_22q11.2 Sindrom distalne delecije 22q11.2 - Wikipedia sindrom wikipedia https://fbri.vtc.vt.edu/events/dissertation-defense/2025-11-24-rukh-shah.html Dissertation Defense: Developmental Origins of Cortical Circuit Dysfunction in a 22q11 Deletion... Nov. 24, 2025, 8 a.m. | Shah Rukh | Graduate Student Dissertation Defense dissertation defense https://pubmed.ncbi.nlm.nih.gov/36672900/ Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions Diagnosis of a chromosome 22q11.2 microdeletion and its associated deletion syndrome (22q11.2DS) is optimally made early. We reviewed the available literature... prenatal screening diagnostic considerations https://pubmed.ncbi.nlm.nih.gov/37541396/ The relationship between oxidative stress and psychotic disorders in 22q11.2 deletion syndrome Our results suggest that dysregulation of OS mechanisms may play a role in the pathophysiology of the 22q11.2DS phenotype. The 22q11.2DS individuals with... https://cordis.europa.eu/project/id/268298 NEUROGENESIS IN 22Q11.2 DELETION SYNDROME: ROLE OF microRNAs | MIRNAS/22Q11DS | Project | Fact... The 22q11.2 deletion syndrome (22qDS) is the most common hemizygous microdeletion syndrome occurring in humans. Individuals with 22qDS show also a variety of... https://researchprofiles.ku.dk/da/publications/schizophrenia-spectrum-disorders-in-a-danish-22q112-deletion-synd/ Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total... https://scholars.duke.edu/publication/933213 Scholars@Duke publication: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and... https://22q11europe.org/ 22Q11 Europe - 22q11 Europe. A supranational European network about the 22q11 deletion syndrome 22q11 Europe. A supranational European network about the 22q11 deletion syndrome european network about the supranational deletion syndrome https://3tonderzoek.sites.uu.nl/informatie/taalontwikkelingsstoornis-tos/ 3T onderzoek: Taal, 22q11 en TOS | Taalontwikkelingsstoornis (TOS) Wilt u meer te weten komen over taalontwikkelingsstoornissen, oftewel TOS? Op de website Alles over TOS is informatie te vinden over TOS. Deze website is... onderzoek taal en tos https://scholars.duke.edu/publication/912189 Scholars@Duke publication: A study of the neuropsychological manifestations in children with 22q11... https://pure.psu.edu/en/publications/narrowing-the-critical-region-for-a-rhabdoid-tumor-locus-in-22q11/ Narrowing the critical region for a rhabdoid tumor locus in 22q11 - Penn State