Open Access Highly Accessed Case report

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

Emmanouil Manolakos*, Sandro Orru, Rosita Neroutsou, Konstantinos Kefalas, Eirini Louizou, Ioannis Papoulidis, Loretta Thomaidis, Panagiotis Peitsidis, Sotirios Sotiriou, George Kitsos, Panagiota Tsoplou, Michael B Petersen and Aikaterini Metaxotou

Molecular Cytogenetics 2009, 2:26 doi:10.1186/1755-8166-2-26

Correction to typographical error

Michael B. Petersen   (2010-03-06 15:50)  Eurogenetica SA email

"We apologize for the typographical error in the cited reference [5] in the published manuscript. "Mattina T, Concetta SP, Grossfeld P: Jacobsen syndrome. Orphanet J Rare Dis 2009, 4:9" should read "Mattina T, CS Perrotta, Grossfeld P: Jacobsen syndrome. Orphanet J Rare Dis 2009, 4:9"

Competing interests

None declared

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