Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements
Author:
Publisher
Wiley
Subject
Psychiatry and Mental health,Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health
Reference70 articles.
1. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features
2. Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome
3. High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
4. Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion
5. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
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