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Updated: Jan 7, 2026

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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
Published on: December 1, 2017
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Las variantes de novo MAP2K4 causan un nuevo síndrome de desarrollo neurológico con alteración de la señalización JNK
medRxiv : the preprint server for health sciences
|January 2, 2026
Resumen
No abstract available in PubMed .
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