Yale Scientists Identify New Genes Related to Congenital Hydrocephalus < Yale School of Medicine
Figure 2 from Congenital hydrocephalus in clinical practice: a genetic diagnostic approach. | Semantic Scholar
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus | Nature Medicine
Genetic Deletion of Afadin Causes Hydrocephalus by Destruction of Adherens Junctions in Radial Glial and Ependymal Cells in the Midbrain | PLOS ONE
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus | Nature Neuroscience
Practical Horse Genetics (Australia)
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions - ScienceDirect
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene | Acta Neuropathologica Communications | Full Text
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
Multi-omic analysis elucidates the genetic basis of hydrocephalus - ScienceDirect
JCM | Free Full-Text | Reappraisal of Pediatric Normal-Pressure Hydrocephalus
Characterization of Rfx4 +/-mice with hydrocephalus. (A) H&E staining.... | Download Scientific Diagram
Frontiers | Diagnostic Approach to Macrocephaly in Children
Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
Navigating the ventricles: Novel insights into the pathogenesis of hydrocephalus - ScienceDirect
Genetics of Hydrocephalus (HC)
The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017 - Annals of Neurology - Wiley Online Library
Metabolic Disorders | NGS Panels: centogene.com
a) The hydrocephalus trait was transmitted to the next generation in... | Download Scientific Diagram
Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis - José Pedro Vieira, Patricia Lopes, Rita Silva, 2012
Frontiers | Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3
Multi-omic analysis elucidates the genetic basis of hydrocephalus
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance | Human Genomics | Full Text