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Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10‐formyltetrahydrofolate dehydrogenase - Naz - 2016 - Journal of Neurochemistry - Wiley Online Library
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Characterization of Rfx4 +/-mice with hydrocephalus. (A) H&E staining.... | Download Scientific Diagram
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Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort | SpringerLink
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NTM meningitis, presenting as hydrocephalus, in a 30-year-old male.... | Download Scientific Diagram
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Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions - ScienceDirect
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Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance | Human Genomics | Full Text
Genetic Deletion of Afadin Causes Hydrocephalus by Destruction of Adherens Junctions in Radial Glial and Ependymal Cells in the Midbrain | PLOS ONE
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Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus | Nature Medicine
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Figure 2 from Congenital hydrocephalus in clinical practice: a genetic diagnostic approach. | Semantic Scholar
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The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017 - Annals of Neurology - Wiley Online Library
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Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis - José Pedro Vieira, Patricia Lopes, Rita Silva, 2012
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus
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Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus | Nature Neuroscience
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Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus | Scientific Reports
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