Familial syndrome of progressive arterial occlusive disease consistent with fibromuscular dysplasia, hypertension, congenital cardiac defects, bone fragility, brachysyndactyly, and learning disabilities.

Source:http://linkedlifedata.com/resource/pubmed/id/9489789

Am. J. Med. Genet. 1998 Feb 17 75 5 469-80

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PMID
9489789