Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: ZIC3[original query] |
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Genetic variants in ZIC1, ZIC2, and ZIC3 are not major risk factors for neural tube defects in humans. American journal of medical genetics. Part A 2004 Jan 124A (1): 40-7. Klootwijk Riko, Groenen Pascal, Schijvenaars Mascha, Hol Frans, Hamel Ben, Straatman Huub, Steegers-Theunissen Régine, Mariman Edwin, Franke Barba |
Lack of association between ZIC2 and ZIC3 genes and the risk of neural tube defects (NTDs) in Hispanic populations. American journal of medical genetics. Part A 2003 Feb 116A (4): 414-5. Zhu Huiping, Junker Wade M, Finnell Richard H, Brown Stephen, Shaw Gary M, Lammer Edward J, Canfield Mark, Hendricks Ka |
Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle. American journal of medical genetics. Part A 2013 Apr 161A (4): 792-802. D'Alessandro Lisa C A, Latney Brande C, Paluru Prasuna C, Goldmuntz Elizabe |
Genetic and functional analyses of ZIC3 variants in congenital heart disease. Human mutation 2014 Jan 35 (1): 66-75. Cowan Jason, Tariq Muhammad, Ware Stephanie |
Analysis of mutations in 7 candidate genes for dextro-Transposition of the great arteries in Chinese population. Journal of thoracic disease 2014 May 6 (5): 491-6. Lei Liming, Lin Haoming, Zhong Shilong, Zhang Zhiwei, Chen Jimei, Li Xin-Xin, Yu Xiyong, Liu Xaioqing, Zhuang Ji |
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Human mutation 2015 Aug . Hilger Alina C, Halbritter Jan, Pennimpede Tracie, van der Ven Amelie, Sarma Georgia, Braun Daniela A, Porath Jonathan D, Kohl Stefan, Hwang Daw-Yang, Dworschak Gabriel C, Hermann Bernhard G, Pavlova Anna, El-Maarri Osman, Nöthen Markus M, Ludwig Michael, Reutter Heiko, Hildebrandt Friedhe |
Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease. Journal of human genetics 2015 Oct . Yoshida Akiko, Morisaki Hiroko, Nakaji Mai, Kitano Masataka, Kim Ki-Sung, Sagawa Koichi, Ishikawa Shiro, Satokata Ichiro, Mitani Yoshihide, Kato Hitoshi, Hamaoka Kenji, Echigo Shigeyuki, Shiraishi Isao, Morisaki Takayu |
Genetic architecture of laterality defects revealed by whole exome sequencing. European journal of human genetics : EJHG 2019 1 27 (4): 563-573. Li Alexander H, Hanchard Neil A, Azamian Mahshid, D'Alessandro Lisa C A, Coban-Akdemir Zeynep, Lopez Keila N, Hall Nancy J, Dickerson Heather, Nicosia Annarita, Fernbach Susan, Boone Philip M, Gambin Tomaz, Karaca Ender, Gu Shen, Yuan Bo, Jhangiani Shalini N, Doddapaneni HarshaVardhan, Hu Jianhong, Dinh Huyen, Jayaseelan Joy, Muzny Donna, Lalani Seema, Towbin Jeffrey, Penny Daniel, Fraser Charles, Martin James, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Ware Stephanie M, Belmont John |
Rapid response of stage IV colorectal cancer with APC/TP53/KRAS mutations to FOLFIRI and Bevacizumab combination chemotherapy: a case report of use of liquid biopsy. BMC medical genetics 2020 1 21 (1): 3. Hendricks Alexander, Rosenstiel Philip, Hinz Sebastian, Burmeister Greta, Röcken Christoph, Boersch Kathrin, Schafmayer Clemens, Becker Thomas, Franke Andre, Forster Micha |
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation. Birth defects research 2022 4 114 (10): 478-486. Thiem Corina E, Stegmann Jil D, Hilger Alina C, Waffenschmidt Lea, Bendixen Charlotte, Köllges Ricarda, Schmiedeke Eberhard, Schäfer Frank-Mattias, Lacher Martin, Kosch Ferdinand, Grasshoff-Derr Sabine, Kabs Carmen, Neser Jörg, Jenetzky Ekkehart, Fazaal Julia, Schumacher Johannes, Hoefele Julia, Ludwig Kerstin U, Reutter Hei |
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis 2022 12 43 (3): 275-279. Wang Yu, Dai Xiaohui, Liu Hanmin, Peng Jin, Chen Ji |
Detection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects. Pharmacogenomics and personalized medicine 2023 3 16 173-181. Cai Rongqin, Tan Ya, Wang Mingming, Yu Huijun, Wang Jing, Ren Zhuo, Dong Zhe, He Yiwen, Li Zhi, Lin Li, Gu Yi |
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- Page last updated:Mar 25, 2024
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