Iain Mclntosh

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Recent reports have described a distinct and recurrent pattern of systemic malformation that associates craniosynostosis and neurodevelop-mental abnormalities with many clinical features of the Marfan syndrome (MFS) 1–7, an autosomal dominant disorder of the extracellular microfibril caused by defects in the gene encoding fibrillin-1, FBN1(ref. 8).(More)
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