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Publications by Trinh Hermanns-Le
Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen
American Journal of Human Genetics
Genetics
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Ehlers-Danlos Syndrome, Classical Type
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Hypermobile Ehlers-Danlos Syndrome (a.k.a. Ehlers-Danlos Syndrome Type III and Ehlers-Danlos Syndrome Hypermobility Type): Clinical Description and Natural History
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A Single Base Mutation in COL5A2 Causes Ehlers-Danlos Syndrome Type II.
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Survival Is Affected by Mutation Type and Molecular Mechanism in Vascular Ehlers–Danlos Syndrome (EDS Type IV)
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Chronic Fatigue in Ehlers-Danlos Syndrome-Hypermobile Type
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Hypermobile Ehlers Danlos Syndrome
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Ehlers-Danlos Syndrome Type IV With Bilateral Pneumothorax
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Ehlers-Danlos Syndrome Type IV, Vascular Type, Which Demonstrated a Novel Point Mutation in the COL3A1 Gene
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Early-Onset Osteoarthritis in Ehlers-Danlos Syndrome Type VIII
American Journal of Medical Genetics, Part A
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