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1-7 of 7 results for 22q11 microdeletion syndrome

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Open access

Research article

First published 2020

Optimising immunisation in children with 22q11 microdeletion

Angela Berkhout, Kahn Preece, Vanil Varghese [...]

Therapeutic Advances in Vaccines and Immunotherapy

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Research article

First published 2007-03

A Novel,Single Nucleotide Polymorphism-Based Assay to Detect 22q11 Deletions

Birgit H. Funke, Alison C. Brown, Marco F. Ramoni [...]

Genetic Testing and Molecular Biomarkers

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Other

First published 2004-05

Frontal and Caudate Alterations in Velocardiofacial Syndrome (Deletion at Chromosome 22q11.2)

Wendy R. Kates, Courtney P. Burnette, Brandy A. Bessette [...]

Journal of Child Neurology

Retricted access

Research article

First published 2011-09

Cryptic Chromosomal Rearrangements in Children with Idiopathic Mental Retardation in the Czech Population

Katerina Hirschfeldova, Alice Baxova, Vera Kebrdlova [...]

Genetic Testing and Molecular Biomarkers

Open access

Review article

First published 2014-6

A Synaptic Function Approach to Investigating Complex Psychiatric Diseases

Laurie R. Earls, Stanislav S. Zakharenko

The Neuroscientist

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Case report

First published 2014-9

Neuropathology of 22q11 Deletion Syndrome in an Infant

Peter Wu, Lisa Teot, Geoffrey Murdoch [...]

Pediatric and Developmental Pathology

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Research article

First published 2012-12

Startle reactivity and prepulse inhibition of the acoustic startle response are modulated by catechol- O -methyl-transferase Val 158 Met polymorphism in adults with 22q11 deletion syndrome

Mariken B de Koning, Erik Boot, Oswald JN Bloemen [...]

Journal of Psychopharmacology