Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: GCNT2[original query] |
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Role of rare germline copy number variation in melanoma-prone patients. Future oncology (London, England) 2016 Mar . Fidalgo Felipe, Rodrigues Tatiane Cristina, Silva Amanda Gonçalves, Moredo Facure Luciana, de Sá Bianca Costa Soares, Duprat João Pedreira, Achatz Maria Isabel, Rosenberg Carla, Carraro Dirce Maria, Krepischi Ana Cristina Victori |
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia. G3 (Bethesda, Md.) 2017 8 7 (10): 3257-3268. Javadiyan Shari, Craig Jamie E, Souzeau Emmanuelle, Sharma Shiwani, Lower Karen M, Mackey David A, Staffieri Sandra E, Elder James E, Taranath Deepa, Straga Tania, Black Joanna, Pater John, Casey Theresa, Hewitt Alex W, Burdon Kathryn |
Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract. Orphanet journal of rare diseases 2018 6 13 (1): 94. Li Jingyan, Leng Yunji, Han Shirui, Yan Lulu, Lu Chaoxia, Luo Yang, Zhang Xue, Cao Lih |
Identification of de novo mutations in prenatal neurodevelopment-associated genes in schizophrenia in two Han Chinese patient-sibling family-based cohorts. Translational psychiatry 2020 Sep 10 (1): 307. Jiang Shan, Zhou Daizhan, Wang Yin-Ying, Jia Peilin, Wan Chunling, Li Xingwang, He Guang, Cao Dongmei, Jiang Xiaoqian, Kendler Kenneth S, Tsuang Ming, Mize Travis, Wu Jain-Shing, Lu Yimei, He Lin, Chen Jingchun, Zhao Zhongming, Chen Xiangni |
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- Page last updated:Apr 22, 2024
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