Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D von Molin, Arnaud, Lemoine, Sandrine, Kaufmann, Martin, Breton, Pierre, Nowoczyn, Marie, Ballandonne, Celine, Coudray, Nadia, Mittre, Herve, Richard, Nicolas, Ryckwaert, Amelie, Lavillaureix, Alinoe, Jones, Glenville, Bacchetta, Justine, Kottler, Marie-Laure

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Paternal GNAS Mutations Lead to Severe Intrauterine Growth Retardation (IUGR) and Provide Evidence for a Role of XLαs in Fetal Development von Richard, Nicolas, Molin, Arnaud, Coudray, Nadia, Rault-Guillaume, Pauline, Jüppner, Harald, Kottler, Marie-Laure

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Vitamin D–Dependent Rickets Type 1B (25‐Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition? von Molin, Arnaud, Wiedemann, Arnaud, Demers, Nick, Kaufmann, Martin, Do Cao, Jérémy, Mainard, Laurent, Dousset, Brigitte, Journeau, Pierre, Abeguile, Geneviève, Coudray, Nadia, Mittre, Hervé, Richard, Nicolas, Weryha, Georges, Sorlin, Arthur, Jones, Glenville, Kottler, Marie‐Laure, Feillet, Francois

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A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A/B GNAS and Autosomal Dominant Pseudohypoparathyroidism Type Ib von Richard, Nicolas, Abeguilé, Genevieve, Coudray, Nadia, Mittre, Hervé, Gruchy, Nicolas, Andrieux, Joris, Cathebras, Pascal, Kottler, Marie-Laure

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High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B von Colson, Cindy, Decamp, Matthieu, Gruchy, Nicolas, Coudray, Nadia, Ballandonne, Céline, Bracquemart, Claire, Molin, Arnaud, Mittre, Hervé, Takatani, Rieko, Jüppner, Harald, Kottler, Marie-Laure, Richard, Nicolas

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Maternal Transmission Ratio Distortion of GNAS Loss‐of‐Function Mutations von Snanoudj, Sarah, Molin, Arnaud, Colson, Cindy, Coudray, Nadia, Paulien, Sylvie, Mittre, Hervé, Gérard, Marion, Schaefer, Elise, Goldenberg, Alice, Bacchetta, Justine, Odent, Sylvie, Naudion, Sophie, Demeer, Bénédicte, Faivre, Laurence, Gruchy, Nicolas, Kottler, Marie‐Laure, Richard, Nicolas

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Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia von Molin, Arnaud, Nowoczyn, Marie, Coudray, Nadia, Ballandone, Céline, Abéguilé, Geneviève, Mittre, Hervé, Richard, Nicolas, Eckart, Philippe, Castanet, Mireille, Kottler, Marie-Laure

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mtDNA Legacy of the Levantine Early Upper Palaeolithic in Africa von Olivieri, Anna, Achilli, Alessandro, Pala, Maria, Battaglia, Vincenza, Fornarino, Simona, Al-Zahery, Nadia, Scozzari, Rosaria, Cruciani, Fulvio, Behar, Doron M, Dugoujon, Jean-Michel, Coudray, Clotilde, Santachiara-Benerecetti, A. Silvana, Semino, Ornella, Bandelt, Hans-Jürgen, Torroni, Antonio

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Timing of a Back-Migration into Africa [with Response] von Forster, Peter, Romano, Valentino, Olivieri, Anna, Achilli, Alessandro, Pala, Maria, Battaglia, Vincenza, Fornarino, Simona, Al-Zahery, Nadia, Scozzari, Rosaria, Cruciani, Fulvio, Behar, Doron M., Dugoujon, Jean-Michel, Coudray, Clotilde, Santachiara-Benerecetti, A. Silvana, Semino, Ornella, Bandelt, Hans-Jürgen, Torroni, Antonio

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