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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Pelger-Huët anomaly in a child with 1q42.3-44 deletion

Theodosia A Kalfa1, Sherri A Zimmerman, Barbara K Goodman

  • 1Hematology-Oncology, Cincinnati Children's Hospital Medical Center, The University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA. theodosia.kalfa@cchmc.org

Pediatric Blood & Cancer
|July 12, 2005
PubMed

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