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Κατακτώ Υπνοδωμάτιο σημείο τομής hydrocephalus gene panel χαλαρώστε την ψυχραιμία Ανθολογία ελάχιστο
Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
Loss of Zebrafish lgi1b Leads to Hydrocephalus and Sensitization to Pentylenetetrazol Induced Seizure-Like Behavior | PLOS ONE
The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017 - Annals of Neurology - Wiley Online Library
Infantile hydrocephalus: a review of epidemiology, classification and causes. | Semantic Scholar
Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
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
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions - ScienceDirect
a) The hydrocephalus trait was transmitted to the next generation in... | Download Scientific Diagram
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus | Scientific Reports
Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus | SpringerLink
Aggravated hydrocephalus of NTM meningitis. (Upper panel) After 1... | Download Scientific Diagram
Unlocking the genetic complexity of congenital hydrocephalus | Nature Medicine
Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort | SpringerLink
Deletions in CWH43 cause idiopathic normal pressure hydrocephalus | EMBO Molecular Medicine
Genetic Mutations and their Role in Congenital Hydrocephalus
Practical Horse Genetics (Australia)
Multi-omic analysis elucidates the genetic basis of hydrocephalus - ScienceDirect
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene | Acta Neuropathologica Communications | Full Text
Genetics of Hydrocephalus (HC)
Frontiers | Diagnostic Approach to Macrocephaly in Children
X-linked Hydrocephalus (L1 Syndrome) | MedLink Neurology
NTM meningitis, presenting as hydrocephalus, in a 30-year-old male.... | Download Scientific Diagram
IJMS | Free Full-Text | Novel Insight in Idiopathic Normal Pressure Hydrocephalus (iNPH) Biomarker Discovery in CSF
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