Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: CLTCL1[original query] |
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Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus. BMC medical genetics 2011 Dec 12 (1): 1. Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, Sun HJ, Bao LM, Shen J, Fu QH, Li F, Sun K |
Exome sequencing of oral squamous cell carcinoma in users of Arabian snuff reveals novel candidates for driver genes. International journal of cancer 2016 Mar . Al-Hebshi Nezar Noor, Li Shiyong, Nasher Akram Thabet, El-Setouhy Maged, Alsanosi Rashad, Blancato Jan, Loffredo Christoph |
Candidate genes of oculo-auriculo-vertebral spectrum in 22q region: A systematic review. American journal of medical genetics. Part A 2020 9 182 (11): 2624-2631. Glaeser Andressa Barreto, Santos Andressa Schneiders, Diniz Bruna Lixinski, Deconte Desireé, Rosa Rafael Fabiano Machado, Zen Paulo Ricardo Gazzo |
Germline Variants in Cancer Genes from Young Breast Cancer Mexican Patients. Cancers 2022 4 14 (7): . Gómez-Flores-Ramos Liliana, Barraza-Arellano Angélica Leticia, Mohar Alejandro, Trujillo-Martínez Miguel, Grimaldo Lizbeth, Ortiz-Lopez Rocío, Treviño Víct |
Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect. Genes 2023 4 14 (4): . Caiyun Zhu, Yang Yang, Bo Pan, Hui Wei, Jiahang Ju, Nuo Si, Qi |
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- Page last updated:Jun 03, 2024
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