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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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14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and

Celeste C Eno1, Jesper Graakjaer2, Dea Svaneby2

  • 1Department of Academic Pathology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

American Journal of Medical Genetics. Part A
|February 26, 2021
PubMed

Keywords:
CALM1PSMC1RPS6KA5TTC7Bdevelopmental delaymicrodeletion 14q32.11

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