Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: SALL4[original query] |
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Mutational analysis of SAL-Like 4 (SALL4) in Han Chinese women with premature ovarian failure. Molecular human reproduction 2009 Sep 15 (9): 557-62. Wang Binbin, Li Lin, Ni Feng, Song Junjie, Wang Jing, Mu Yuan, Ma Xu, Cao Yunx |
Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect. International journal of cardiology 2010 Nov 145 (2): 224-6. Wang Binbin, Li Lin, Xie Xiaodong, Wang Jing, Yan Jinting, Mu Yuan, Ma |
Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies. American journal of medical genetics. Part A 2012 Oct 158A (10): 2463-72. Browne Marilyn L, Carter Tonia C, Kay Denise M, Kuehn Devon, Brody Lawrence C, Romitti Paul A, Liu Aiyi, Caggana Michele, Druschel Charlotte M, Mills James |
ß-catenin alteration is rare in hepatocellular carcinoma with steatohepatitic features: immunohistochemical and mutational study. Virchows Archiv : an international journal of pathology 2015 Aug . Ando Sumiyo, Shibahara Junji, Hayashi Akimasa, Fukayama Masas |
The expression of SALL4 is significantly associated with EGFR, but not KRAS or EML4-ALK mutations in lung cancer. Journal of thoracic disease 2016 Oct 8 (10): 2682-2688. Jia Xiangbo, Qian Rulin, Zhang Binbin, Zhao So |
Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome?wide association study. Molecular medicine reports 2017 Aug . Yamada Yoshiji, Sakuma Jun, Takeuchi Ichiro, Yasukochi Yoshiki, Kato Kimihiko, Oguri Mitsutoshi, Fujimaki Tetsuo, Horibe Hideki, Muramatsu Masaaki, Sawabe Motoji, Fujiwara Yoshinori, Taniguchi Yu, Obuchi Shuichi, Kawai Hisashi, Shinkai Shoji, Mori Seijiro, Arai Tomio, Tanaka Masas |
A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles. BMC research notes 2017 Nov 10 (1): 562. Abu-Amero Khaled K, Kondkar Altaf A, Khan Arif |
Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations. Human genetics 2019 1 138 (1): 83-92. Wang Qiqi, Li Da, Cai Baozhu, Chen Qing, Li Caihua, Wu Yanhua, Jin Li, Wang Xiuxia, Zhang Xiaojin, Zhang Fe |
A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Frontiers in pediatrics 2020 7 8 310. van de Putte Romy, Dworschak Gabriel C, Brosens Erwin, Reutter Heiko M, Marcelis Carlo L M, Acuna-Hidalgo Rocio, Kurtas Nehir E, Steehouwer Marloes, Dunwoodie Sally L, Schmiedeke Eberhard, Märzheuser Stefanie, Schwarzer Nicole, Brooks Alice S, de Klein Annelies, Sloots Cornelius E J, Tibboel Dick, Brisighelli Giulia, Morandi Anna, Bedeschi Maria F, Bates Michael D, Levitt Marc A, Peña Alberto, de Blaauw Ivo, Roeleveld Nel, Brunner Han G, van Rooij Iris A L M, Hoischen Alexand |
Genome-Wide Association Study for the Identification of Novel Genetic Variants Associated with the Risk of Neuroblastoma in Korean Children.
Cancer research and treatment 2020 Oct 52 (4): 1251-1261. Bae Joon Seol, Lee Ji Won, Yoo Jung Eun, Joung Je-Gun, Yoo Keon Hee, Koo Hong Hoe, Song Yun-Mi, Sung Ki Woo |
SMARCA4/BRG1-Deficient Non-Small Cell Lung Carcinomas: A Case Series and Review of the Literature. Archives of pathology & laboratory medicine 2021 Jan 145 (1): 90-98. Nambirajan Aruna, Singh Varsha, Bhardwaj Nishu, Mittal Saurabh, Kumar Sunil, Jain Deepa |
The Classification of VACTERL Association into 3 Groups According to the Limb Defect. Plastic and reconstructive surgery. Global open 2021 3 9 (2): e3360. Al-Qattan Mohammad |
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- Page last updated:Mar 25, 2024
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