Case report

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

Caroline M Ogilvie¹^*, Joo W Ahn¹, Kathy Mann¹, Roland G Roberts² and Frances Flinter³

¹ 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

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

Published: 24 February 2009

Additional file 1:

Table 2. 28 obvious gene-like items.

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