Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CHCHD3[original query] |
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Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Science translational medicine 2011 Aug 3 (95): 95ra75. Lionel Anath C, Crosbie Jennifer, Barbosa Nicole, Goodale Tara, Thiruvahindrapuram Bhooma, Rickaby Jessica, Gazzellone Matthew, Carson Andrew R, Howe Jennifer L, Wang Zhuozhi, Wei John, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Fiebig Andreas, Franke Andre, Schreiber Stefan, Zwaigenbaum Lonnie, Fernandez Bridget A, Roberts Wendy, Arnold Paul D, Szatmari Peter, Marshall Christian R, Schachar Russell, Scherer Stephen |
Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). Rare diseases (Austin, Tex.) 2013 Dec 1 (1): 1. Xie Zhihui, Nagarajan Vijayaraj, Sturdevant Daniel E, Iwaki Shoko, Chan Eunice, Wisch Laura, Young Michael, Nelson Celeste M, Porcella Stephen F, Druey Kirk |
Mitochondrial and Nuclear Mitochondrial Variants in Allergic Diseases. Allergy, asthma & immunology research 2020 Sep 12 (5): 877-884. Jang Haerin, Kim Mina, Hong Jung Yeon, Cho Hyung Ju, Kim Chang Hoon, Kim Yoon Hee, Sohn Myung Hyun, Kim Kyung W |
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