Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Silver-Russell Syndrome and H19[original query] |
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No evidence for mutations of CTCFL/BORIS in Silver-Russell syndrome patients with IGF2/H19 imprinting control region 1 hypomethylation. PloS one 2009 4 (8): e6631. Bernier-Latmani Jeremiah, Baumer Alessandra, Shaw Phill |
No evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age. BMC medical genetics 2014 15 67. Murphy Rinki, Thompson John Md, Tost Jörg, Mitchell Edwin A, |
Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. European journal of human genetics : EJHG 2018 9 27 (1): 42-48. Soellner Lukas, Kraft Florian, Sauer Sabrina, Begemann Matthias, Kurth Ingo, Elbracht Miriam, Eggermann Thom |
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- Page last updated:Apr 29, 2024
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