Marfan syndrome: fibrillin expression and microfibrillar abnormalities in a family with predominant ocular defects. | Journal of Medical Genetics

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Marfan syndrome: fibrillin expression and microfibrillar abnormalities in a family with predominant ocular defects.

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Cite this article as:: Kielty CM, Davies SJ, Phillips JE, et al

Marfan syndrome: fibrillin expression and microfibrillar abnormalities in a family with predominant ocular defects.

Journal of Medical Genetics 1995;32:1-6.