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Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic...
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Hereditary Elliptocytosis in Iceland
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Mild haemophilia A in Iceland: clinical genetic studies of three families with t...
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Mild haemophilia A in Iceland: clinical genetic studies of three families with t...
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Molecular Biology of Hereditary Cystatin C Amyloid Angiopathy in Iceland
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Three RFLP's at the 3' end of the cystatin C gene, the disease gene in hereditar...
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Three RFLPs at the 3′ end of the cystatin C gene, the disease gene in hereditary...
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Three RFLPs at the 3' end of the cystatin C gene, the disease gene in hereditary...
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Three RFLPs at the 3′ end of the cystatin C gene, the disease gene in hereditary...
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Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the br...
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Missense mutations causing mild hemophilia A in Iceland detected by denaturing g...
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Serum amyloid P-component and C-reactive protein in serum of healthy Icelanders...
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Wilson disease in Iceland: a clinical and genetic study
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Wilson disease in Iceland: a clinical and genetic study.
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The first Icelandic family with X-linked agammaglobulinaemia: studies of genetic...
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The application of molecular genetics to detection of craniofacial abnormality.
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Icelandic families with autosomal dominant polycystic kidney disease: families u...
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Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelan...
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Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic f...
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An isolate of families with hereditary cystatin C amyloid angiopathy and cerebra...
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