Skip to content
Descubridor Institucional UMAR
Inicio
Búsqueda avanzada
Explorar
Inicio
Búsqueda avanzada
Explorar
Login
Language
English
Deutsch
Español
Français
Italiano
All Fields
Title
Author
Subject
Call Number
ISBN/ISSN
Tag
Find
Advanced
Contiguous Xp21 Deletion Syndrome with Atypical Phenotype Requires Further Clarification Using WES
Contiguous Xp21 Deletion Syndrome with Atypical Phenotype Requires Further Clarification Using WES
Fuente:
Zenodo
Saved in:
Bibliographic Details
Main Author:
Josef Finsterer
Format:
Recurso digital
Published:
Zenodo
2025
Online Access:
Acceder al recurso
Tags:
Add Tag
No Tags, Be the first to tag this record!
Cite this
Text this
Email this
Print
Export Record
Export to RefWorks
Export to EndNoteWeb
Export to EndNote
Save to List
Permanent link
Holdings
Description
Comments
Similar Items
Staff View
Internet
https://doi.org/10.5281/zenodo.15659880
Similar Items
Pitfalls in Calculating the Incidence of Guillain‐Barre Syndrome During the Pandemic
by: Josef Finsterer
Published: (2025)
COVID‐19 Patients With Neurological Symptoms Require a Neurological Diagnosis and the Establishment of a Causal Relationship
by: Josef Finsterer
Published: (2025)
Homogeneous ALS Cohorts in Terms of Etiology, onset type, and Vaccination Status Are Required to Assess the Outcome of Their COVID Infection
by: Josef Finsterer
Published: (2025)
Leigh Syndrome Due to the Variant c. 1019T >C in COX15
by: Josef Finsterer
Published: (2025)
Treatment of Stroke-Like Episodes Requires NO-Precursors, Avoidance of Mitochondrion Toxic Drugs, and Antiepileptics only When Seizures Occur
by: Josef Finsterer
Published: (2025)