Disease: Chromosome 22- microdeletion 22 q11
- 22q11.2 Microduplication: An Enigmatic Genetic Disorder
- A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome
- Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a <em>de Novo</em> 22q11.1q11.22 Duplication
- An attempt to identify 22q11.2 microdeletions in samples of the Hungarian schizophrenia DNA bank by multiplex ligation-based probe amplification (MLPA): literature review, methodology and results
- Atypical microdeletion in 22q11 deletion syndrome reveals new candidate causative genes: A case report and literature review
- Clinical Features of Aberrations Chromosome 22q: A Pilot Study
- Coding of social novelty in the hippocampal CA2 region and its disruption and rescue in a 22q11.2 microdeletion mouse model
- Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2
- Diagnosis of 22q11.2 deletion syndrome in the context of newly developed psychosis
- Microarray analysis in pregnancies with isolated unilateral kidney agenesis
- Microdeletion 22q11.2 syndrome: Does thymus incidental surgical resection affect its immunological profile?
- Novel Combination of Surface Markers for the Reliable and Comprehensive Identification of Human Thymic Epithelial Cells by Flow Cytometry: Quantitation and Transcriptional Characterization of Thymic Stroma in a Pediatric Cohort
- Prenatal diagnosis and clinical significance of cephalocele-A single institution experience and literature review
- Prenatal ultrasonic characteristics and genetic analysis of fetuses with chromosome 22q11 microdeletion syndrome
- Retropharyngeal lipostructure in the treatment of velopharyngeal insufficiency: A prospective study and update
- Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior
- The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology
- The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome
- Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples