Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes
Leire Madariaga(University of the Basque Country), Laurence Heidet(Hôpital Necker-Enfants Malades), Nathalie Leporrier(Laboratoire de Physique Corpusculaire de Caen), Vincent Morinière(Hôpital Necker-Enfants Malades), Rémi Salomon(Inserm), Raymonde Bouvier, Bruno Turlin(Inserm), Corinne Antignac(Hôpital Necker-Enfants Malades), Marie-Claire Gübler(Inserm), Philippe Loget(Hôpital Pontchaillou), Dominique Gaillard(MACOM (United States)), Marc Jeanpierre(Délégation Paris 5), Jéléna Martinovic(Hôpital Necker-Enfants Malades), Uffe Birk Jensen(Aarhus University Hospital), Christel Thauvin-Robinet(Inserm), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Michèle Mathieu(Hôpital Nord), Pierre Déchelotte(Inserm)
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