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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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A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects

S C Saitta, J M McGrath, H Mensch

    American Journal of Human Genetics
    |July 27, 1999
    PubMed
    Abstract

    No abstract available in PubMed .

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