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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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Alpha128 Arg-->Ser (CGT-->AGT) spectrin mutation associated with severe neonatal elliptopoikilocytosis in Spain

J L Corrons, A Pujades, R Alvarez

    Haematologica
    |June 19, 2001
    PubMed
    Abstract

    No abstract available in PubMed .

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