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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 new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3

O Uyguner1, H Kayserili, Y Li

  • 1Istanbul Medical Faculty, Medical Genetics Department, Istanbul University, Istanbul, Turkey. o.uyguner@istanbul.edu.tr

Clinical Genetics
|February 21, 2007
PubMed

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