HuGE Literature Finder
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Records 1-2
Mutational Spectrum in Holoprosencephaly Shows That Fgf is a New Major Signaling Pathway.
Human mutation 2016 Jul . Dubourg Christèle, Carré Wilfrid, Hamdi-Rozé Houda, Mouden Charlotte, Roume Joëlle, Abdelmajid Benmansour, Amram Daniel, Baumann Clarisse, Chassaing Nicolas, Coubes Christine, Faivre-Olivier Laurence, Ginglinger Emmanuelle, Gonzales Marie, Levy-Mozziconacci Annie, Lynch Sally-Ann, Naudion Sophie, Pasquier Laurent, Poidvin Amélie, Prieur Fabienne, Sarda Pierre, Toutain Annick, Dupé Valérie, Akloul Linda, Odent Sylvie, de Tayrac Marie, David Véroniq |
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
Journal of medical genetics 2009 Jun 46 (6): 389-98. Lacbawan F, Solomon B D, Roessler E, El-Jaick K, Domené S, Vélez J I, Zhou N, Hadley D, Balog J Z, Long R, Fryer A, Smith W, Omar S, McLean S D, Clarkson K, Lichty A, Clegg N J, Delgado M R, Levey E, Stashinko E, Potocki L, Vanallen M I, Clayton-Smith J, Donnai D, Bianchi D W, Juliusson P B, Njølstad P R, Brunner H G, Carey J C, Hehr U, Müsebeck J, Wieacker P F, Postra A, Hennekam R C M, van den Boogaard M-J H, van Haeringen A, Paulussen A, Herbergs J, Schrander-Stumpel C T R M, Janecke A R, Chitayat D, Hahn J, McDonald-McGinn D M, Zackai E H, Dobyns W B, Muenke |
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