Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Delfien Syx
Expanding the Clinical and Mutational Spectrum of the Ehlers–Danlos Syndrome, Dermatosparaxis Type
Genetics in Medicine
Medicine
Genetics
Musculocontractural Ehlers-Danlos Syndrome (Former EDS Type VIB) and Adducted Thumb Clubfoot Syndrome (ATCS) Represent a Single Clinical Entity Caused by Mutations in the Dermatan-4-Sulfotransferase 1 Encoding CHST14 Gene
Human Mutation
Genetics
Related publications
Hypermobile Ehlers-Danlos Syndrome (a.k.a. Ehlers-Danlos Syndrome Type III and Ehlers-Danlos Syndrome Hypermobility Type): Clinical Description and Natural History
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
The Natural History, Including Orofacial Features of Three Patients With Ehlers-Danlos Syndrome, Dermatosparaxis Type (EDS Type VIIC)
American Journal of Medical Genetics
Ehlers-Danlos Syndrome, Classical Type
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
Hypermobile Ehlers Danlos Syndrome
Balkan Medical Journal
Medicine
Anaesthetic Implications of Vascular Type Ehlers-Danlos Syndrome
Anaesthesia and Intensive Care
Critical Care
Anesthesiology
Pain Medicine
Intensive Care Medicine
Ehlers-Danlos Syndrome Type IV With Bilateral Pneumothorax
Internal Medicine
Internal Medicine
Medicine
Chronic Fatigue in Ehlers-Danlos Syndrome-Hypermobile Type
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
Murine Model of the Ehlers-Danlos Syndrome
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Early-Onset Osteoarthritis in Ehlers-Danlos Syndrome Type VIII
American Journal of Medical Genetics, Part A
Genetics