Human Genome Epidemiology Literature Finder
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Query Trace: LETM1[original query] |
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Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts. Human genetics 2015 Nov . Conte Federica, Oti Martin, Dixon Jill, Carels Carine E L, Rubini Michele, Zhou Huiqi |
Whole?exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family. Molecular medicine reports 2020 7 22 (3): 2469-2477. Li Yiqiang, Lin Xuemei, Zhu Mingwei, Li Jingchun, Yuan Zhe, Xu Hongw |
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- Page last updated:Apr 22, 2024
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