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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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Correspondence on "Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome

Yarden S Fraiman1, Monica H Wojcik2

  • 1Department of Neonatology, Beth Israel Deaconess Medical Center, Boston, MA.

Genetics in Medicine : Official Journal of the American College of Medical Genetics
|June 17, 2026
PubMed
Abstract

No abstract available in PubMed .

Keywords:
22qCopy-number variationMicrodeletionOptical mappingRepeats

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