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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

165 related items for PubMed ID: 7111035

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  • 26. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.
    Irrthum A, Karkkainen MJ, Devriendt K, Alitalo K, Vikkula M.
    Am J Hum Genet; 2000 Aug; 67(2):295-301. PubMed ID: 10856194
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  • 33. [Hereditary lymphedema (Milroy's disease). Case contribution].
    Roberi PL, Bini P, Zannino L, Rossi E.
    Minerva Pediatr; 1978 May 31; 30(10):839-44. PubMed ID: 672831
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