Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients
Marie‐France Portnoï(Inserm), Muriel Houang(Inserm), Sandrine Marlin(Hôpital Necker-Enfants Malades), Yves Le Bouc(Inserm), Lina Finkel(Sorbonne Université), Sylvie Odent(Institut de génétique et de développement de Rennes), Françoise Denoyelle(Hôpital Necker-Enfants Malades), Nicolas Gruchy(Laboratoire de Physique Corpusculaire de Caen), Christèle Dubourg(Centre Hospitalier Universitaire de Rennes), Jean‐Pierre Siffroi(Sorbonne Université)
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