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Updated: Aug 19, 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

Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome

Noriko Miyake, Remco Visser, Akira Kinoshita

    American Journal of Medical Genetics. Part A
    |February 22, 2005
    PubMed
    Abstract

    No abstract available in PubMed .

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