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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
08:22

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9pter leads p22 deletion syndrome: a case report

P W Allderdice, W D Heneghan, E T Felismino

    Birth Defects Original Article Series
    |January 1, 1976
    PubMed
    Summary

    No abstract available in PubMed .

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