A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report

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Case report

Caroline Mackie Ogilvie¹ , Joo Wook Ahn¹ , Kathy Mann¹ , Roland G Roberts² and Frances Flinter³

¹Cytogenetics Department, Guy's & St Thomas' NHS Foundation Trust, London, UK

²Department of Medical & Molecular Genetics, King's College London School of Medicine, London, UK

³Genetics Department, Guy's & St Thomas' NHS Foundation Trust, London, UK

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Molecular Cytogenetics 2009, 2:9doi:10.1186/1755-8166-2-9


Published:	24 February 2009

Additional file 1:

Table 2. 28 obvious gene-like items.

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