Search Results - Yann Heuzé

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  1. 1
    Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses

    Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses by Yann Heuzé, G.H. Holmes, Inga Peter, Joan T. Richtsmeier, Ethylin Wang Jabs

    Published 2014
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  2. 2
    FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models

    FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models by Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier

    Published 2011
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  3. 3
    New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis

    New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis by Yann Heuzé, Simeon A. Boyadjiev, Jeffrey L. Marsh, Alex A. Kane, Elijah Cherkez, James E. Boggan, Joan T. Richtsmeier

    Published 2010
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  4. 4
    FGFR3 mutation causes abnormal membranous ossification in achondroplasia

    FGFR3 mutation causes abnormal membranous ossification in achondroplasia by Federico Di Rocco, Martin Biosse Duplan, Yann Heuzé, Nabil Kaci, Davide Komla‐Ebri, Arnold Münnich, Emilie Mugniery, Catherine Benoist-Lasselin, Laurence Legeai‐Mallet

    Published 2014
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  5. 5
    Meckel’s and condylar cartilages anomalies in achondroplasia result in defective development and growth of the mandible

    Meckel’s and condylar cartilages anomalies in achondroplasia result in defective development and growth of the mandible by Martin Biosse Duplan, Davide Komla‐Ebri, Yann Heuzé, Valentin Estibals, Emilie Gaudas, Nabil Kaci, Catherine Benoist-Lasselin, Michel Zérah, Ina Krämer, Michaela Kneissel, Diana Grauss Porta, Federico Di Rocco, Laurence Legeai‐Mallet

    Published 2016
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  6. 6
    Hypochondroplasia gain-of-function mutation in FGFR3 causes defective bone mineralization in mice

    Hypochondroplasia gain-of-function mutation in FGFR3 causes defective bone mineralization in mice by Léa Loisay, Davide Komla‐Ebri, Anne Morice, Yann Heuzé, Camille Viaut, Amélie de La Seiglière, Nabil Kaci, Danny Chan, A. Lamouroux, Geneviève Baujat, J. H. Duncan Bassett, Graham R. Williams, Laurence Legeai‐Mallet

    Published 2023
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  7. 7
    A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

    A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9 by Cristina M. Justice, Garima Yagnik, Yoonhee Kim, Inga Peter, Ethylin Wang Jabs, Mónica Erazo, Xiaoqian Ye, E Ainehsazan, Lisong Shi, Michael L. Cunningham, Virginia Kimonis, Tony Roscioli, Steven A. Wall, Andrew O.M. Wilkie, Joan M. Stoler, Joan T. Richtsmeier, Yann Heuzé, Pedro A. Sanchez‐Lara, Michael F. Buckley, Charlotte M. Druschel, James L. Mills, Michele Caggana, Paul A. Romitti, Denise M. Kay, Craig W. Senders, Peter J. Taub, Ophir D. Klein, James E. Boggan, Marike Zwienenberg-Lee, C. Naydenov, Jin Oh Kim, Alexander F. Wilson, Simeon A. Boyadjiev

    Published 2012
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