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Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease.
Circ Res. 2004 Jun 11;94(11):1429-35. doi: 10.1161/01.RES.0000130528.72330.5c. Epub 2004 Apr 29.
Circ Res. 2004.
PMID: 15117819
An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis.
Somerville MJ, Sprysak KA, Hicks M, Elyas BG, Vicen-Wyhony L.
Somerville MJ, et al.
Am J Hum Genet. 1999 Sep;65(3):924-6. doi: 10.1086/302550.
Am J Hum Genet. 1999.
PMID: 10441599
Free PMC article.
No abstract available.
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