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Updated: Oct 4, 2026

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 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

Smith-Lemli-Opitz (RHS) syndrome: holoprosencephaly and homozygous IVS8-1G-->C genotype

M J Nowaczyk1, S A Farrell, W L Sirkin

  • 1Department of Pathology and Molecular Medicine, McMaster University, Canada. nowaczyk@hhsc.ca

American Journal of Medical Genetics
|September 20, 2001
PubMed

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