Research  

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

Paola Evangelidou, Carolina Sismani, Marios Ioannides, Christodoulos Christodoulou, George Koumbaris, Ioannis Kallikas, Ioannis Georgiou, Voula Velissariou, Philippos C Patsalis Molecular Cytogenetics 2010, 3:24 (26 November 2010)

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Research  

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes

Marilyn L Slovak, David D Smith, Victoria Bedell, Ya-Hsuan Hsu, Margaret O'Donnell, Stephen J Forman, Karl Gaal, Lisa McDaniel, Roger Schultz, Blake C Ballif, Lisa G Shaffer Molecular Cytogenetics 2010, 3:23 (15 November 2010)

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Research  

The use of array-CGH in a cohort of Greek children with developmental delay

Emmanouil Manolakos, Annalisa Vetro, Konstantinos Kefalas, Stamatia-Maria Rapti, Eirini Louizou, Antonios Garas, George Kitsos, Lefteris Vasileiadis, Panagiota Tsoplou, Makarios Eleftheriades, Panagiotis Peitsidis, Sandro Orru, Thomas Liehr, Michael B Petersen, Loretta Thomaidis Molecular Cytogenetics 2010, 3:22 (9 November 2010)

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Research  

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

Judith Frohnauer, Almuth Caliebe, Stefan Gesk, Carl-Joachim Partsch, Reiner Siebert, Rainer Pankau, Jutta Jenderny Molecular Cytogenetics 2010, 3:21 (5 November 2010)

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