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Publications by Philip Vlummens
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
Recent Advances in the Pathophysiology of Musculocontractural Ehlers-Danlos Syndrome
Genes
Genetics
Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen
American Journal of Human Genetics
Genetics
Ehlers-Danlos Syndrome, Classical Type
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
Survival Is Affected by Mutation Type and Molecular Mechanism in Vascular Ehlers–Danlos Syndrome (EDS Type IV)
Genetics in Medicine
Medicine
Genetics
Hypermobile Ehlers Danlos Syndrome
Balkan Medical Journal
Medicine
A Single Base Mutation in COL5A2 Causes Ehlers-Danlos Syndrome Type II.
Journal of Medical Genetics
Genetics
Chronic Fatigue in Ehlers-Danlos Syndrome-Hypermobile Type
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
Ehlers-Danlos Syndrome Type IV With Bilateral Pneumothorax
Internal Medicine
Internal Medicine
Medicine
