Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome
Sood S, Eldadah ZA, Krause WL, et al: Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome. Nat Genet 1996; 12:209-211
Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull
Saal HM, Bulas DI, Allen JF, et al: Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull. Am J Med Genet 1995; 57:573-578
The spectrum of cardiovascular disease in Marfan's syndrome: A clinico-morphologic study of 18 necropsy patients and comparison to 151 previously reported necropsy patients
Roberts WC, Hoing HS: The spectrum of cardiovascular disease in Marfan's syndrome: a clinico-morphologic study of 18 necropsy patients and comparison to 151 previously reported necropsy patients. Am Heart J 1982; 104:115-135
Genetic linkage of the Marfan syndrome, ectopic lentis, and congenital contractual arachnodactyly to the fibrillin genes on chromosomes 15 and 5
Tsipouras P, Del Mastro R, Sarfarazi M, et al: Genetic linkage of the Marfan syndrome, ectopic lentis, and congenital contractual arachnodactyly to the fibrillin genes on chromosomes 15 and 5. N Engl J Med 1992; 326:905-909