Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and FOXC2[original query] |
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| 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, |
| Forkhead box C2 promoter variant c.-512C>T is associated with increased susceptibility to chronic venous diseases. PloS one 2014 9 (3): e90682. Surendran Sumi, Girijamma Athira, Nair Radhakrishnan, Ramegowda Kalpana S, Nair Divya H, Thulaseedharan Jissa V, Lakkappa Ravikumar B, Kamalapurkar Giridhar, Kartha Chandrasekharan |
| Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome. Journal of genetics 2019 6 98 (2): . Wang Enshi, Nie Yu, Fan Xuesong, Zheng Zhe, Gu Haiyong, Zhang Hao, Hu Shengsh |
| Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma. PloS one 2019 1 14 (1): e0211029. Medina-Trillo Cristina, Aroca-Aguilar José-Daniel, Ferre-Fernández Jesús-José, Alexandre-Moreno Susana, Morales Laura, Méndez-Hernández Carmen-Dora, García-Feijoo Julián, Escribano Jul |
| Improvement of quality of life by intake of hydroxytyrosol in patients with lymphedema and association of lymphedema genes with obesity. European review for medical and pharmacological sciences 2021 12 25 (1 Suppl): 33-42. Dhuli K, Ceccarini M R, Precone V, Maltese P E, Bonetti G, Paolacci S, Dautaj A, Guerri G, Marceddu G, Beccari T, Michelini S, Bertelli |
| Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
- Page last reviewed:Feb 1, 2024
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