Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and GH1[original query] |
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| Genetic polymorphisms in the human growth hormone-1 gene (GH1) and the risk of breast carcinoma. Cancer 2004 Jul 101 (2): 251-7. Ren Zefang, Cai Qiuyin, Shu Xiao-Ou, Cai Hui, Cheng Jia-Rong, Wen Wan-Qing, Gao Yu-Tang, Zheng W |
| Association between fetal growth restriction and polymorphisms at sites -1 and +3 of pituitary growth hormone: a case-control study. BMC pregnancy and childbirth 2005 Feb 5 (1): 2. Adkins Ronald M, Campese Caroline, Vaidya Rehana, Boyd Theonia |
| Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke. Human genetics 2006 Jun 119 (5): 527-40. Horan Martin, Newsway Vicky, Yasmin , Lewis Mark D, Easter Tammy E, Rees D Aled, Mahto Arti, Millar David S, Procter Annie M, Scanlon Maurice F, Wilkinson Ian B, Hall Ian P, Wheatley Amanda, Blakey John, Bath Philip M W, Cockcroft John R, Krawczak Michael, Cooper David |
| Polymorphisms in the pituitary growth hormone gene and its receptor associated with coronary artery disease in a predisposed cohort from India. Journal of genetics 2010 Dec 89 (4): 437-47. Maitra Arindam, Shanker Jayashree, Dash Debabrata, Sannappa Prathima R, John Shibu, Siwach Pratibha, Rao Veena S, Sridhara H, Kakkar Vijay |
| Association analysis of ten candidate genes in a large multinational cohort of small for gestational age children and children with idiopathic short stature (NESTEGG study). Hormone research in pædiatrics 2013 80 (6): 466-76. de Graaff L C G, Clark A J L, Tauber M, Ranke M B, Johnston L B, Caliebe J, Molinas C, Amin N, van Duijn C, Wollmann H, Wallaschofski H, Savage M O, Hokken-Koelega A C |
| Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism. Clinical endocrinology 2015 1 82 (6): 876-84. Fritez Nabila, Sobrier Marie-Laure, Iraqi Hinde, Vié-Luton Marie-Pierre, Netchine Irène, El Annas Abdessamad, Pantel Jacques, Collot Nathalie, Rose Sophie, Piterboth William, Legendre Marie, Chraibi Abdelmjid, Amselem Serge, Kadiri Abdelkrim, Hilal Lati |
| Genetic determinants of growth hormone and GH-related phenotypes. BMC genomics 2017 Oct 18 (1): 822. Hallengren Erik, Almgren Peter, Svensson Malin, Gallo Widet, Engström Gunnar, Persson Margaretha, Melander Ol |
| IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. European journal of endocrinology 2022 10 187 (6): 787-795. Fourneaux Rachel, Reynaud Rachel, Mougel Gregory, Castets Sarah, Bretones Patricia, Dauriat Benjamin, Edouard Thomas, Raverot Gerald, Barlier Anne, Brue Thierry, Castinetti Frederic, Saveanu Alexand |
| Clinical and genetic evaluation of children with short stature of unknown origin. BMC medical genomics 2023 8 16 (1): 194. Qianqian Zhao, Yanying Li, Qian Shao, Chuanpeng Zhang, Shuang Kou, Wanling Yang, Mei Zhang, Bo B |
| [A prospective study of genetic screening of 2 060 neonates by high-throughput sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 5 40 (6): 641-647. Danyan Zhuang, Fei Wang, Shuxia Ding, Zhoushu Zheng, Qi Yu, Lanqiu Lyu, Shuni Sun, Rulai Yang, Wenwen Que, Haibo |
| Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes. Archives of endocrinology and metabolism 2023 11 68 e220254. Tar?k K?rkgöz, Semra Gürsoy, Sezer Acar, Özlem Nalbanto?lu, Beyhan Özkaya, Hüseyin An?l Korkmaz, Filiz Hazan, Behzat Özk |
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