Molecular Cytogenetics

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Open Access 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

Author Affiliations

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 files

Additional file 1:

Table 2. 28 obvious gene-like items.

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