Human Genome Epidemiology Literature Finder

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Query Trace: Disease and DVL2[original query]
A Rare Rs139365823 Polymorphism in Pre-miR-138 Is Associated with Risk of Congenital Heart Disease in a Chinese Population. DNA and cell biology 2018 Jan . Gao Xiaobo, Yang Liping, Luo Haiyan, Tan Fengwei, Ma Xu, Lu Caili Similar articles in PubMed
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability. HGG advances 2022 1 3 (1): 100074. Zhang Chaofan, Jolly Angad, Shayota Brian J, Mazzeu Juliana F, Du Haowei, Dawood Moez, Soper Patricia Celestino, Ramalho de Lima Ariadne, Ferreira Bárbara Merfort, Coban-Akdemir Zeynep, White Janson, Shears Deborah, Thomson Fraser Robert, Douglas Sarah Louise, Wainwright Andrew, Bailey Kathryn, Wordsworth Paul, Oldridge Mike, Lester Tracy, Calder Alistair D, Dumic Katja, Banka Siddharth, Donnai Dian, Jhangiani Shalini N, Potocki Lorraine, Chung Wendy K, Mora Sara, Northrup Hope, Ashfaq Myla, Rosenfeld Jill A, Mason Kati, Pollack Lynda C, McConkie-Rosell Allyn, Kelly Wei, McDonald Marie, Hauser Natalie S, Leahy Peter, Powell Cynthia M, Boy Raquel, Honjo Rachel Sayuri, Kok Fernando, Martelli Lucia R, Filho Vicente Odone, Genomics England Research Consortium , Muzny Donna M, Gibbs Richard A, Posey Jennifer E, Liu Pengfei, Lupski James R, Sutton V Reid, Carvalho Claudia M Similar articles in PubMed
The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis. Journal of cardiovascular development and disease 2024 7 11 (7): . Olga Irtyuga, Rostislav Skitchenko, Mary Babakekhyan, Dmitrii Usoltsev, Svetlana Tarnovskaya, Anna Malashicheva, Yulya Fomicheva, Oksana Rotar, Olga Moiseeva, Ulyana Shadrina, Mykyta Artomov, Anna Kostareva, Evgeny Shlyakh Similar articles in PubMed