Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: CCBE1[original query] |
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Multilocus analysis of GAW15 NARAC chromosome 18 case-control data. BMC proceedings 2007 1 Suppl 1 S11. Browning Sharon R, Thomas Jessi |
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Molecular syndromology 2013 Sep 4 (6): 257-66. Mendola A, Schlögel M J, Ghalamkarpour A, Irrthum A, Nguyen H L, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken J B, Boon L M, Brouillard P, Vikkula M, |
Phenotype and Genotype of a Cohort of Chinese Children with Early-Onset Protein-Losing Enteropathy. The Journal of pediatrics 2019 3 208 38-42.e3. Ye Ziqing, Huang Ying, Wang Yuhuan, Lu Junping, Wu Jie, Yu Zhuow |
Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American journal of medical genetics. Part A 2019 10 182 (1): 189-194. Boone Philip M, Paterson Scott, Mohajeri Kiana, Zhu Wenmiao, Genetti Casie A, Tai Derek J C, Nori Neeharika, Agrawal Pankaj B, Bacino Carlos A, Bi Weimin, Talkowski Michael E, Hogan Benjamin M, Rodan Lance |
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