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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 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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Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on

M G Tanamy1, N Magal, G J Halpern

  • 1Department of Molecular Genetics, Felsenstein Medical Research Center, Rabin Medical Center, Petah Tikva, Israel.

American Journal of Medical Genetics
|December 18, 2001
PubMed

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