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    • European Reference Networks
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    • How to Cite ERN-ITHACA in Your Publications?
    • ILIAD
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    • ERN-ITHACA Patients Representatives
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    • Patients Documentation
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    • Online Genetics Course APOGeE
    • Guidelines
    • Orphanet Updates
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    • EuroDysmorpho
    • International meeting on Rubinstein-Taybi Syndrome
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Home > For Clinicians > 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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