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This previously undescribed phenotype represents yet another in the widening spectrum of fibrillinopathies caused by an <jats:italic>FBN1<\/jats:italic> gene mutation. \u00a9 2002 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.10333","type":"journal-article","created":{"date-parts":[[2002,8,25]],"date-time":"2002-08-25T23:45:33Z","timestamp":1030319133000},"page":"261-270","source":"Crossref","is-referenced-by-count":30,"title":["Segregation of a novel <i>FBN1<\/i> gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations"],"prefix":"10.1002","volume":"109","author":[{"given":"Lesley 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