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Journal Abstract Search

132 related items for PubMed ID: 36170577

  • 1. Compound heterozygosity for a variably penetrant variant and a variant of unknown significance in FLT4 causes fully penetrant Milroy's lymphedema.
    Kim J, Lim SY.
    Lymphology; 2022; 55(2):41-46. PubMed ID: 36170577
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  • 4. Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation.
    Mizuno S, Yamada Y, Yamada K, Nomura N, Wakamatsu N.
    Congenit Anom (Kyoto); 2005 Jun; 45(2):59-61. PubMed ID: 15904433
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  • 5. A novel VEGFR3 mutation causes Milroy disease.
    Butler MG, Dagenais SL, Rockson SG, Glover TW.
    Am J Med Genet A; 2007 Jun 01; 143A(11):1212-7. PubMed ID: 17458866
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  • 6. Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3.
    Spiegel R, Ghalamkarpour A, Daniel-Spiegel E, Vikkula M, A Shalev S.
    J Hum Genet; 2006 Jun 01; 51(10):846-850. PubMed ID: 16924388
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  • 8. Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.
    Gordon K, Schulte D, Brice G, Simpson MA, Roukens MG, van Impel A, Connell F, Kalidas K, Jeffery S, Mortimer PS, Mansour S, Schulte-Merker S, Ostergaard P.
    Circ Res; 2013 Mar 15; 112(6):956-60. PubMed ID: 23410910
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  • 10. Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.
    Connell FC, Ostergaard P, Carver C, Brice G, Williams N, Mansour S, Mortimer PS, Jeffery S, Lymphoedema Consortium.
    Hum Genet; 2009 Jan 15; 124(6):625-31. PubMed ID: 19002718
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  • 11. Case Report: The compound heterozygotes variants in FLT4 causes autosomal recessive hereditary lymphedema in a Chinese family.
    Xiang Q, Chen J, Xiao X, Xu B, Xie H, Wang H, Yang M, Liu S.
    Front Genet; 2023 Jan 15; 14():1140406. PubMed ID: 37035731
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  • 12. A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema.
    Melikhan-Revzin S, Kurolap A, Dagan E, Mory A, Gershoni-Baruch R.
    Lymphat Res Biol; 2015 Jun 15; 13(2):107-11. PubMed ID: 26091405
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  • 14. A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.
    Liu NF, Yu Z, Luo Y, Sun D, Yan Z.
    Lymphology; 2015 Jun 15; 48(2):93-6. PubMed ID: 26714373
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  • 15. A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A.
    Sui Y, Lu Y, Lin M, Ni X, Chen X, Li H, Jiang M.
    BMC Med Genomics; 2021 Jun 08; 14(1):151. PubMed ID: 34103024
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  • 16. Rare Variants in LAMA5 Gene associated with FLT4 and FOXC2 Mutations in Primary Lymphedema May Contribute to Severity.
    Liu NF, Yu ZY, Sun D, Lou Y.
    Lymphology; 2016 Dec 08; 49(4):192-204. PubMed ID: 29908552
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  • 17. Investigation on the role of biallelic variants in VEGF-C found in a patient affected by Milroy-like lymphedema.
    Mukenge S, Jha SK, Catena M, Manara E, Leppänen VM, Lenti E, Negrini D, Bertelli M, Brendolan A, Jeltsch M, Aldrighetti L.
    Mol Genet Genomic Med; 2020 Sep 08; 8(9):e1389. PubMed ID: 32592340
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  • 18. FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.
    Gordon K, Spiden SL, Connell FC, Brice G, Cottrell S, Short J, Taylor R, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.
    Hum Mutat; 2013 Jan 08; 34(1):23-31. PubMed ID: 23074044
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