Fibulin-2: Genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2

European Journal of Human Genetics

Volumn 4, Issue 5, 1996, Pages 292-295

  Collod, Gwenaëlle ^a  

^a INSERM   (France)

Author keywords

Extra cellular matrix protein; Fibulin; Marfan syndrome

Indexed keywords

FIBULIN; SCLEROPROTEIN;

ARTICLE; CHROMOSOME 3P; CLINICAL ARTICLE; CONTROLLED STUDY; EXTRACELLULAR MATRIX; FEMALE; GENE MAPPING; GENE SEQUENCE; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; HEREDITARY CONNECTIVE TISSUE DISEASE; HUMAN; HUMAN CELL; MALE; MARFAN SYNDROME; PHENOTYPE; PRIORITY JOURNAL;

EID: 0029910971     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472216     Document Type: Article

References (2)

1. Pyeritz RE: The Marfan syndrome; in Royce PM, Steinmann B (eds): Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects. New York, Wiley-Liss 1993, pp 437-468.
2. Boileau C, Jondeau G, Babron M-C, Coulon M, Alexandre J-A, Sakai L, Melki J, Delorme G, Dubourg O, Bonaïti-Pellié C, Bourdarias J-P, Junien C: Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes. Am J Hum Genet 1993;53:46-54.