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Updated: May 15, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1

Rob Van Zwieten, Jerney J J M François, Karin Van Leeuwen

    American Journal of Hematology
    |December 21, 2012
    PubMed
    Abstract

    No abstract available in PubMed .

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