Show
Sort by
-
Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndrome
-
COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers-Danlos syndrome
-
Ehlers-Danios syndromes and Marfan syndrome
-
The molecular basis of classic Ehlers-Danlos syndrome: A comprehensive study of biochemical and molecular findings in 48 unrelated patients
-
Rationalised ACE inhibition (ACE-I) dosing in non-hypertensive children
-
The natural history of human dermatosparaxis (Ehlers-Danios Syndrome VII C)