Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Hirschsprung Disease and PHOX2B[original query] |
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| PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome. American journal of human genetics 2005 Mar 76 (3): 421-6. Trochet Delphine, O'Brien Louise M, Gozal David, Trang Ha, Nordenskjöld Agneta, Laudier Béatrice, Svensson Pär-Johan, Uhrig Sabine, Cole Trevor, Niemann Stephan, Munnich Arnold, Gaultier Claude, Lyonnet Stanislas, Amiel Jean |
| The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype. Chest 2005 Jan 127 (1): 72-9. Trang Ha, Dehan Michel, Beaufils François, Zaccaria Isabelle, Amiel Jeanne, Gaultier Claude, |
| Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China. Journal of pediatric surgery 2009 Sep 44 (9): 1805-11. Liu Cui-Ping, Li Xin-Gang, Lou Jin-Tu, Xue Yun, Luo Chun-Fen, Zhou Xue-Wu, Chen Fei, Li Xiang, Li Meng, Li Ji-Che |
| Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome. Journal of human genetics 2015 Sep 60 (9): 473-7. Shimokaze Tomoyuki, Sasaki Ayako, Meguro Toru, Hasegawa Hisaya, Hiraku Yuka, Yoshikawa Tetsushi, Kishikawa Yumiko, Hayasaka Kiyos |
| Pleiotropic effect of common PHOX2B variants in Hirschsprung disease and neuroblastoma. Aging 2019 2 11 (4): 1252-1261. Zhao Jinglu, Zhu Yun, Xie Xiaoli, Yao Yuxiao, Zhang Jiao, Zhang Ruizhong, Huang Lihua, Cheng Jiwen, Xia Huimin, He Jing, Zhang Y |
| Novel PHOX2B mutations in congenital central hypoventilation syndrome. Pediatrics international : official journal of the Japan Pediatric Society 2019 2 61 (4): 393-396. Sasaki Ayako, Kishikawa Yumiko, Imaji Reisuke, Fukushima Yu, Nakamura Yukiko, Nishimura Yutaka, Yamada Megumi, Mino Yoichi, Mitsui Tetsuo, Hayasaka Kiyos |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
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