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Publications by J B Harrison
A Single Base Mutation in COL5A2 Causes Ehlers-Danlos Syndrome Type II.
Journal of Medical Genetics
Genetics
Related publications
A Novel Missense Mutation of COL5A2 in a Patient With Ehlers–Danlos Syndrome
Human Genome Variation
Biochemistry
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Molecular Biology
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
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
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Chronic Fatigue in Ehlers-Danlos Syndrome-Hypermobile Type
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
Hypermobile Ehlers Danlos Syndrome
Balkan Medical Journal
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Ehlers-Danlos Syndrome Type IV With Bilateral Pneumothorax
Internal Medicine
Internal Medicine
Medicine
Ehlers-Danlos Syndrome Type IV, Vascular Type, Which Demonstrated a Novel Point Mutation in the COL3A1 Gene
Internal Medicine
Internal Medicine
Medicine
Ehlers-Danlos Syndrome and Periventricular Nodular Heterotopia in a Spanish Family With a Single FLNA Mutation
Journal of Medical Genetics
Genetics
