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Translational Psychiatry|February 19, 2020
Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathologySinead Morrison, Samuel J R A Chawner, Therese A M J van Amelsvoort, et al.
American Journal of Human Genetics|October 3, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic RearrangementsWolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
Human Molecular Genetics|December 30, 2019
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic originsLisanne Vervoort, Wolfram Demaerel, Laura Y Rengifo, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 4, 2019
Low prevalence of substance use in people with 22q11.2 deletion syndromeClaudia Vingerhoets, Mathilde J F van Oudenaren, Oswald J N Bloemen, et al.
Research Square|January 9, 2026
Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndromeCaren Latrèche, Valentina Mancini, Marija Dvojakovska, et al.
Neurology|May 13, 2018
Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2Erik Boot, Nancy J Butcher, Sean Udow, et al.
The American Journal of Psychiatry|July 29, 2017
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeAnne S Bassett, Chelsea Lowther, Daniele Merico, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
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