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This page is a summary of: A three-generation family with terminal microdeletion involving 5p15.33–32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome, European Journal of Medical Genetics, March 2014, Elsevier,
DOI: 10.1016/j.ejmg.2014.02.005.
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