The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017 - Annals of Neurology - Wiley Online Library
a) The hydrocephalus trait was transmitted to the next generation in... | Download Scientific Diagram
Metabolic Disorders | NGS Panels: centogene.com
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus | Nature Neuroscience
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance | Human Genomics | Full Text
Unlocking the genetic complexity of congenital hydrocephalus | Nature Medicine
Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
Characterization of Rfx4 +/-mice with hydrocephalus. (A) H&E staining.... | Download Scientific Diagram
Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions - ScienceDirect
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus
Genetic Mutations and their Role in Congenital Hydrocephalus
Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis - José Pedro Vieira, Patricia Lopes, Rita Silva, 2012
JCM | Free Full-Text | Reappraisal of Pediatric Normal-Pressure Hydrocephalus
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene | Acta Neuropathologica Communications | Full Text
Ependymal ciliary motion and their role in congenital hydrocephalus | SpringerLink
IJMS | Free Full-Text | Novel Insight in Idiopathic Normal Pressure Hydrocephalus (iNPH) Biomarker Discovery in CSF
Genetics of Hydrocephalus (HC)
Figure 2 from Congenital hydrocephalus in clinical practice: a genetic diagnostic approach. | Semantic Scholar
Frontiers | Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3
Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus | SpringerLink
X-linked Hydrocephalus (L1 Syndrome) | MedLink Neurology
Multi-omic analysis elucidates the genetic basis of hydrocephalus - ScienceDirect
