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Updated: Jul 17, 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

Familial occurrence of syngnathia congenita syndrome

I Gassner, W Müller, H Rössler

    Clinical Genetics
    |March 1, 1979
    PubMed

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