Case reportA novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report1 Cytogenetics Department, Guy's & St Thomas' NHS Foundation Trust, London, UK 2 Department of Medical & Molecular Genetics, King's College London School of Medicine, London, UK 3 Genetics Department, Guy's & St Thomas' NHS Foundation Trust, London, UK
Molecular Cytogenetics 2009, 2:9doi:10.1186/1755-8166-2-9
Additional filesAdditional file 1: Table 2. 28 obvious gene-like items. Format: DOC Size: 121KB Download file This file can be viewed with: Microsoft Word Viewer |





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