Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: HLX[original query] |
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Functional polymorphisms in TBX21 and HLX are associated with development and prognosis of Graves' disease. Autoimmunity 2012 Mar 45 (2): 129-36. Morita Mami, Watanabe Mikio, Inoue Naoya, Inaoka Chisa, Akamizu Takashi, Tatsumi Ke-Ita, Hidaka Yoh, Iwatani Yoshino |
De novo copy number variants are associated with congenital diaphragmatic hernia. Journal of medical genetics 2012 Oct 49 (10): 650-9. Yu Lan, Wynn Julia, Ma Lijiang, Guha Saurav, Mychaliska George B, Crombleholme Timothy M, Azarow Kenneth S, Lim Foong Yen, Chung Dai H, Potoka Douglas, Warner Brad W, Bucher Brian, LeDuc Charles A, Costa Katherine, Stolar Charles, Aspelund Gudrun, Arkovitz Marc S, Chung Wendy |
Variants in the IFN? transcription factor genes TBET, STAT1, STAT4, and HLX and the risk of pulmonary tuberculosis in a Colombian population: a case-control study. Biomédica : revista del Instituto Nacional de Salud 0 33 (2): 259-67. Sánchez Dulfary, Lefebvre Céline, García Luis F, Barrera Luis |
Systematic analysis of copy number variation associated with congenital diaphragmatic hernia. Proceedings of the National Academy of Sciences of the United States of America 2018 05 115 (20): 5247-5252. Zhu Qihui, High Frances A, Zhang Chengsheng, Cerveira Eliza, Russell Meaghan K, Longoni Mauro, Joy Maliackal P, Ryan Mallory, Mil-Homens Adam, Bellfy Lauren, Coletti Caroline M, Bhayani Pooja, Hila Regis, Wilson Jay M, Donahoe Patricia K, Lee Charl |
Impact of Human Genetic Variation on C-Reactive Protein Concentrations and Acute Appendicitis. Frontiers in immunology 2022 13 862742. Ricaño-Ponce Isis, Peeters Toon, Matzaraki Vasiliki, Houben Bert, Achten Ruth, Cools Peter, Netea Mihai G, Gyssens Inge C, Kumar Vin |
Rs868058 in the Homeobox Gene HLX Contributes to Early-Onset Fetal Growth Restriction. Biology 2022 3 11 (3): . Wujcicka Wioletta Izabela, Kacerovsky Marian, Krekora Micha?, Kaczmarek Piotr, Le?niczak Beata, Grzesiak Mariu |
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