Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Intestinal Obstruction and RET[original query] |
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Gdnf haploinsufficiency causes Hirschsprung-like intestinal obstruction and early-onset lethality in mice. American journal of human genetics 2002 1 70 (2): 435-47. Shen Liya, Pichel José G, Mayeli Thomas, Sariola Hannu, Lu Bai, Westphal Hein |
Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2. European journal of human genetics : EJHG 2004 Aug 12 (8): 604-12. Burzynski Grzegorz M, Nolte Ilja M, Osinga Jan, Ceccherini Isabella, Twigt Bas, Maas Saskia, Brooks Alice, Verheij Joke, Plaza Menacho Ivan, Buys Charles H C M, Hofstra Robert M |
Novel mutations of RET gene in Korean patients with sporadic Hirschsprung's disease. Journal of pediatric surgery 2006 Jul 41 (7): 1250-4. Kim Jeong-Hyun, Yoon Kyong-Oh, Kim Jeong-Kook, Kim Jong-Won, Lee Suk-Koo, Kong Sun-Young, Seo Jeong-Me |
The correlation of genetic markers with anatomoclinical and histopathological forms in Hirschsprung's disease. Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2010 51 (2): 283-8. Broasc? V, Ciobotaru Camelia, Dimofte Iuliana, A?chie Mariana, Prun? A, Severin Beatri |
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Human molecular genetics 2016 Oct . Tang Clara Sze-Man, Gui Hongsheng, Kapoor Ashish, Kim Jeong-Hyun, Luzón-Toro Berta, Pelet Anna, Burzynski Grzegorz, Lantieri Francesca, So Man-Ting, Berrios Courtney, Shin Hyoung Doo, Fernández Raquel M, Le Thuy-Linh, Verheij Joke B G M, Matera Ivana, Cherny Stacey S, Nandakumar Priyanka, Cheong Hyun Sub, Antiñolo Guillermo, Amiel Jeanne, Seo Jeong-Meen, Kim Dae-Yeon, Oh Jung-Tak, Lyonnet Stanislas, Borrego Salud, Ceccherini Isabella, Hofstra Robert M W, Chakravarti Aravinda, Kim Hyun-Young, Sham Pak Chung, Tam Paul K H, Garcia-Barceló Maria-Mer |
GT-repeat extension in the IL11 promoter is associated with Hirschsprung's disease (HSCR). Gene 2018 Jul . Haase Michael G, Schulze Annekatrin, Grover Sandeep, Kemnitz Ivonne, König Inke R, Fitze Gui |
High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung's disease. Pediatric surgery international 2024 1 40 (1): 38. Hui-Yang Ding, Wen Lei, Shang-Jie Xiao, Hua Deng, Li-Ke Yuan, Lu Xu, Jia-Liang Zhou, Rong Huang, Yuan-Long Fang, Qing-Yuan Wang, Ying Zhang, Liang Zhang, Xiao-Chun Z |
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- Page last updated:May 20, 2024
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