Skip to main navigation
Skip to search
Skip to main content
University of Luebeck Home
English
Deutsch
Home
Research Units
Experts
Publications
Projects
Datasets
Prizes
Spin-Offs
Activities
Media
Search by expertise, name or affiliation
Klinik und Genetik des Joubert-syndroms
Translated title of the contribution
:
Clinical features and genetics of Joubert syndrome
Y. Hellenbroich
*
, S. K. Frost, G. Gillessen-Kaesbach
*
Corresponding author for this work
Institute of Human Genetics
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Clinical features and genetics of Joubert syndrome'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Medicine and Dentistry
Clinical Feature
100%
Joubert Syndrome
100%
Congenital Malformation
20%
Magnetic Resonance Imaging
20%
Liver Fibrosis
20%
Breathing Pattern
20%
Developmental Delay
20%
Hypotonia
20%
Coloboma
20%
Molar Tooth
20%
Retina Dystrophy
20%
Hindbrain
20%
Nephronophthisis
20%
X Chromosome Linked Disorder
20%
Eye Movement Disorder
20%
Ataxia
20%
Autosomal Recessive Inheritance
20%
Ciliopathy
20%
Biochemistry, Genetics and Molecular Biology
Eye Movement
100%
Autosomal Recessive Inheritance
100%
Magnetic Resonance Imaging
100%
Cilium
100%
Breathing Pattern
100%