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A 2q24.3q31.1 microdeletion found in a patient with Filippi‐like syndrome phenotype: A case report
Authors:Joanna Lazier  Judy Chernos  R. Brian Lowry
Affiliation:1. Department of Medical Genetics, Alberta Children's Hospital, University of Calgary, Calgary, Alberta;2. Cytogenetic Laboratory, Alberta Children's Hospital, University of Calgary, Calgary, Alberta;3. Department of Pediatrics, Alberta Children's Hospital, University of Calgary, Calgary, Alberta;4. Alberta Children's Hospital Research Institute for Child and Maternal Health, Calgary, Alberta
Abstract:
Keywords:Filippi syndrome  2q deletion  syndactyly  chromosome deletion  growth disorders  comparative genomic hybridization  genes  homeobox  hand abnormalities
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