Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery

By Ziolkowska Lidia  

European Journal of Pediatrics, Vol. 167, Iss. 10, 2008-10 ,pp. : 1135-1140

Springer Publishing Company

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A rare association of interrupted aortic arch type C and microdeletion 22q11.2

By Cuturilo Goran  

European Journal of Pediatrics, Vol. 167, Iss. 10, 2008-10 ,pp. : 1195-1198

Springer Publishing Company

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A child with chromosome 22q11.2 deletion syndrome and a bilobed gallbladder

By Clarke James   Schmidt Matthias   Macken Marian   Morley Charlotte   Cummings Elizabeth  

Pediatric Radiology, Vol. 37, Iss. 2, 2007-02 ,pp. : 213-215

Springer Publishing Company

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Evans Syndrome in a Patient with Chromosome 22q11.2 Deletion Syndrome: A Case Report

By Kratz Christian P.   Niehues Tim   Lyding Sigrid   Heusch Andreas   Janssen Gisela   Göbel Ulrich  

Pediatric Hematology and Oncology, Vol. 20, Iss. 2, 2003-03 ,pp. : 167-172

Informa Healthcare

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Frequency of thrombocytopenia and large platelets correlates neither with conotruncal cardiac anomalies nor immunological features in the chromosome 22q11.2 deletion syndrome

By Latger-Cannard Véronique   Bensoussan Danièle   Grégoire Marie-Josée   Marcon François   Cloez Jean-Louis   Leheup Bruno   Jonveaux Philippe   Lecompte Thomas   Bordigoni Pierre  

European Journal of Pediatrics, Vol. 163, Iss. 6, 2004-06 ,pp. : 327-328

Springer Publishing Company

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