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Updated: Jul 3, 2026

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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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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Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome

K Salavoura1, A Kolialexi, C Sofocleous

  • 1Department of Medical Genetics, Athens University School of Medicine, Athens, Greece.

Genetic Counseling (Geneva, Switzerland)
|July 16, 2008
PubMed

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