Search Results - De Langhe, S.P.

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  1. 1
    A genetic mechanism for cecal atresia: the role of the Fgf10 signaling pathway

    A genetic mechanism for cecal atresia: the role of the Fgf10 signaling pathway by Fairbanks, T.J., Kanard, R.C., De Langhe, S.P., Sala, F.G., Del Moral, P.M., Warburton, D., Anderson, K.D., Bellusci, S., Burns, R.C.

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    Deletion of fibroblast growth factor receptor 2b (Fgfr2b) gene results in anorectal malformation in mouse

    Deletion of fibroblast growth factor receptor 2b (Fgfr2b) gene results in anorectal malformation in mouse by Fairbanks, T.J., Kanard, R.C., De Langhe, S.P., Sala, F.G., Anderson, K.D., Warburton, D., Bellusci, S., Burns, R.C.

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    A nonvascular cause of intestinal atresia in fibroblast growth factor receptor 2b mutant

    A nonvascular cause of intestinal atresia in fibroblast growth factor receptor 2b mutant by Fairbanks, T.J., Kanard, R.C., Sala, F.G., De Langhe, S.P., Anderson, K.D., Warburton, D., Bellusci, S., Burns, R.C.

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