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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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DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter

L Moynihan1, M Houseman, V Newton

  • 1Molecular Medicine Unit, University of Leeds, St James's University Hospital, UK.

European Journal of Human Genetics : EJHG
|April 10, 1999
PubMed

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