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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Disease and CYR61[original query]
CCN1 mutation is associated with atrial septal defect.
Pediatric cardiology 2015 Feb 36 (2): 295-9.
Perrot Andreas, Schmitt Katharina R, Roth Eva-Maria G, Stiller Brigitte, Posch Maximilian G, Browne Edmund N L, Timmann Christian, Horstmann Rolf D, Berger Felix, Özcelik Cem
Association of BTG2, CYR61, ZFP36, and SCD gene polymorphisms with Graves' disease and ophthalmopathy.
Thyroid : official journal of the American Thyroid Association 2014 Jul 24 (7): 1156-61.
Planck Tereza, Shahida Bushra, Sjögren Marketa, Groop Leif, Hallengren Bengt, Lantz Mika
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