• A family with many cases of marfanoid hypermobility syndrome
• Aortic disruption after operation for pectus excavatum in a infant with Marfanoid hypermobility syndrome
• Arachnodactyly--a key to diagnosing heritable disorders of connective tissue
• Cardiovascular abnormalities in the Marfanoid hypermobility syndrome
• Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]
• Ehlers-Danlos syndrome type VIII: periodontitis, easy bruising, marfanoid habitus, and distinctive facies
• Engineered mutations in fibrillin-1 leading to Marfan syndrome act at the protein, cellular and organismal levels
• Epidemiology of general joint hypermobility and basis for the proposed criteria for benign joint hypermobility syndrome: review of the literature
• Hypermobile Ehlers-Danlos Syndrome
• IgM Deficiency Associated With Connexin Mutation in an 18-Year-old Male
• Marfanoid hypermobility caused by an 862 kb deletion of Xq22.3 in a patient with Sotos syndrome
• Marfanoid hypermobility syndrome
• Marfanoid hypermobility syndrome and skeletal abnormalities in a rare case of torsion of wandering spleen
• Marfanoid hypermobility syndrome associated with coarctation of the aorta
• Marfanoid hypermobility syndrome associated with Duane's retraction syndrome
• Marfanoid hypermobility syndrome associated with flail mitral valve
• Marfanoid Hypermobility Syndrome: Reminscising a Forgotten Entity
• Marfanoid Hypermobility Syndrome: Reminscising a Forgotten Entity…
• Mitral valve prolapse and joint hypermobility: evidence for a systemic connective tissue abnormality?
• Prevalence of generalised joint hypermobility in school-aged children from east-central European region
• Prophylactiv use of propranolol in the Marfan syndrome to prevent aortic dissection
• Pulmonary lesions seen in a family with Marfanoid hypermobility syndrome
• Pulmonary non-tuberculous mycobacterial infection in congenital contractural arachnodactyly
• Rare Cases of PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome in a Korean Family Identified by Next Generation Sequencing
• Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type
• Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndrome
• Shprintzen-Goldberg syndrome: fourteen new patients and a clinical analysis
• Simultaneous pupil expansion and displacement for femtosecond laser-assisted cataract surgery in patients with lens ectopia
• Surgically treated case of Marfanoid hypermobility syndrome
• Temporomandibular joint dysfunction syndrome: a close association with systemic joint laxity (the hypermobile joint syndrome)
• The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2
• The marfanoid hypermobility syndrome
• The Marfanoid hypermobility syndrome
• The prevalence of joint hypermobility among high school students