Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the

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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
08:22

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

J H Knoll1, R D Nicholls, R E Magenis

  • 1Division of Genetics, Children's Hospital, Boston, MA 02115.

American Journal of Medical Genetics
|February 1, 1989
PubMed

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