Author:
Adès Lesley C.,Holman Katherine J.,Brett Maggie S.,Edwards Matthew J.,Bennetts Bruce
Funder
The Children's Hospital at Westmead (to L.C.A.)
University of Sydney (to L.C.A.)
Financial Markets Foundation for Children (to L.C.A.)
Western Sydney Genetics Program (to L.C.A.)
Marfan Association Victoria, Inc. (to L.C.A.)
Marfan Association Australia (N.S.W. branch) (to L.C.A.)
Subject
Genetics (clinical),Genetics
Reference45 articles.
1. Characterisation of four novel fibrillin-1 (FBN1) mutations in Marfan syndrome;Adès;J Med Genet,1996
2. Aortic dissection, patent ductus arteriosus, iris hypoplasia, and brachytelephalangy in a male adolescent;Adès;Clin Dysmorphol,1999
3. Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of a vertebral dysplasia in three generations;Adès;Am J Med Genet,2002
4. Autosomal recessive ectopia lentis in two Arabic family pedigrees;al Salem;Ophthalmic Pediatr Genet,1990
5. Fibrillin abnormalities and prognosis in Marfan syndrome and related disorders;Aoyama;Am J Med Genet,1995
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