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Home > Printer-friendly > A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.

A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation. [1]

TitoloA case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.
Publication TypeJournal Article
AuthorsFabretto, A [2], Shardlow, A [3], Faletra, F [4], Lepore, L [5], Hladnik, U [6], Gasparini, P [7]
PubMed ID20450314 [8]

Source URL: https://www.burlo.trieste.it/ricerca/pubblicazioni/case-lymphedema-distichiasis-syndrome-carrying-new-de-novo-frameshift-foxc2-mutation#comment-0

Collegamenti
[1] https://www.burlo.trieste.it/ricerca/pubblicazioni/case-lymphedema-distichiasis-syndrome-carrying-new-de-novo-frameshift-foxc2-mutation
[2] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=401
[3] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=406
[4] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=407
[5] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=408
[6] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=409
[7] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=211
[8] http://www.ncbi.nlm.nih.gov/pubmed/20450314?dopt=Abstract