Search Results - Grevoul-Fesquet, Julie

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  1. 1
    Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita

    Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita by Weber, Mathilde, Jaber, Dana, Encha‐Razavi, Ferechte, Julien, Emmanuel, Grevoul‐Fesquet, Julie, Steffann, Julie, Melki, Judith, Martinovic, Jelena

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  2. 2
    The First Fetal Case of Shwachman-Diamond Syndrome Mimicking Vascular Growth Restriction

    The First Fetal Case of Shwachman-Diamond Syndrome Mimicking Vascular Growth Restriction by Bobric, Nicoleta-Andreea, Grevoul-Fesquet, Julie, Rigonnot, Luc, Trost, Detlef, Boughalem, Aïcha, Martinovic, Jelena

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    First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15

    First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15 by Receveur, Aline, Puisney-Dakhli, Chloé, Kleinfinger, Pascale, Gitz, Laurence, Grevoul-Fesquet, Julie, Jouni, Dima, Diot, Romain, Tachdjian, Gérard, Petit, François

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