Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2

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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

Rika Kosaki1, Kenjiro Kosaki, Kazushige Matsushima

  • 1Division of Medical Genetics, Saitama Children's Medical Center, Saitama 339-551, Japan.

Congenital Anomalies
|May 21, 2005
PubMed

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