Publication | Open Access

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

Terminal MicrodeletionSteady PhenotypeDevelopmental BiologyMendelian DisorderCytogeneticsGenetic DisorderGeneticsPathologyThree-generation FamilyMolecular GeneticsChromosomal RearrangementMedicineChromosome 9