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    • Guidelines & consensus (WG11)
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Home > Our Research Activities > List Of Publications > Rare and de novo coding variants in chromodomain genes in Chiari I malformation

Rare and de novo coding variants in chromodomain genes in Chiari I malformation

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Manic and Depressive Symptoms in Children Diagnosed with Noonan Syndrome
Melanotic Neuroectodermal Tumor of Infancy (MNTI) and Pineal Anlage Tumor (PAT) Harbor A Medulloblastoma Signature by DNA Methylation Profiling
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