Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
IJMS | Free Full-Text | Novel Insight in Idiopathic Normal Pressure Hydrocephalus (iNPH) Biomarker Discovery in CSF
Multi-omic analysis elucidates the genetic basis of hydrocephalus - ScienceDirect
Characterization of Rfx4 +/-mice with hydrocephalus. (A) H&E staining.... | Download Scientific Diagram
Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort | SpringerLink
Multi-omic analysis elucidates the genetic basis of hydrocephalus
Figure 2 from Congenital hydrocephalus in clinical practice: a genetic diagnostic approach. | Semantic Scholar
Unlocking the genetic complexity of congenital hydrocephalus | Nature Medicine
Ependymal ciliary motion and their role in congenital hydrocephalus | SpringerLink
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus | Scientific Reports
Yale Scientists Identify New Genes Related to Congenital Hydrocephalus < Yale School of Medicine
Practical Horse Genetics (Australia)
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
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus | Nature Medicine
Aggravated hydrocephalus of NTM meningitis. (Upper panel) After 1... | Download Scientific Diagram
Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus | SpringerLink
JCM | Free Full-Text | Reappraisal of Pediatric Normal-Pressure Hydrocephalus
Genetic Deletion of Afadin Causes Hydrocephalus by Destruction of Adherens Junctions in Radial Glial and Ependymal Cells in the Midbrain | PLOS ONE
The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017 - Annals of Neurology - Wiley Online Library
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance | Human Genomics | Full Text
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions - ScienceDirect
Deletions in CWH43 cause idiopathic normal pressure hydrocephalus | EMBO Molecular Medicine
Metabolic Disorders | NGS Panels: centogene.com
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus | Nature Neuroscience
