Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: DSTYK[original query] |
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Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract. Journal of the American Society of Nephrology : JASN 2017 May . Heidet Laurence, Morinière Vincent, Henry Charline, De Tomasi Lara, Reilly Madeline Louise, Humbert Camille, Alibeu Olivier, Fourrage Cécile, Bole-Feysot Christine, Nitschké Patrick, Tores Frédéric, Bras Marc, Jeanpierre Marc, Pietrement Christine, Gaillard Dominique, Gonzales Marie, Novo Robert, Schaefer Elise, Roume Joëlle, Martinovic Jelena, Malan Valérie, Salomon Rémi, Saunier Sophie, Antignac Corinne, Jeanpierre Céci |
Identification of 8 Novel Mutations in Nephrogenesis-Related Genes in Chinese Han Patients with Unilateral Renal Agenesis. American journal of nephrology 2017 Jun 46 (1): 55-63. Wu Hangdi, Xu Qian, Xie Jingyuan, Ma Jun, Qiao Panpan, Zhang Wen, Yu Haijin, Wang Weiming, Qian Ying, Zhang Qianying, Guo Yiqing, Tang Yonghua, Chen Xiao-Nong, Wang Zhaohui, Chen N |
Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID study.
Human molecular genetics 2022 4 31 (18): 3021-3031. Pereira Alexandre C, Bes Taniela M, Velho Mariliza, Marques Emanuelle, Jannes Cintia E, Valino Karina R, Dinardo Carla L, Costa Silvia F, Duarte Alberto J S, Santos Alexandre R, Mitne-Neto Miguel, Medina-Pestana Jose, Krieger Jose |
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