Search Results - Bloch-Zupan, Agnès

Otodental syndrome by Bloch-Zupan, Agnès, Goodman, Jane R

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Amelogenesis imperfecta by Crawford, Peter JM, Aldred, Michael, Bloch-Zupan, Agnes

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Clinical utility gene card for: hypophosphatasia by Mornet, Etienne, Beck, Christine, Bloch-Zupan, Agnès, Girschick, Hermann, Le Merrer, Martine

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Clinical utility gene card for: Hypophosphatasia – update 2013 by Mornet, Etienne, Hofmann, Christine, Bloch-Zupan, Agnès, Girschick, Hermann, Le Merrer, Martine

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Molars and incisors: show your microarray IDs by Laugel-Haushalter, Virginie, Paschaki, Marie, Thibault-Carpentier, Christelle, Dembelé, Doulaye, Dollé, Pascal, Bloch-Zupan, Agnès

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Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review by Hejlesen, Jane, Underbjerg, Line, Gjørup, Hans, Bloch-Zupan, Agnes, Sikjaer, Tanja, Rejnmark, Lars, Haubek, Dorte

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Orodental phenotype and genotype findings in all subtypes of hypophosphatasia by Reibel, Amélie, Manière, Marie-Cécile, Clauss, François, Droz, Dominique, Alembik, Yves, Mornet, Etienne, Bloch-Zupan, Agnès

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Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects by Morkmued, Supawich, Laugel-Haushalter, Virginie, Mathieu, Eric, Schuhbaur, Brigitte, Hemmerlé, Joseph, Dollé, Pascal, Bloch-Zupan, Agnès, Niederreither, Karen

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Phenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a model by Marangoni, Pauline, Charles, Cyril, Tafforeau, Paul, Laugel-Haushalter, Virginie, Joo, Adriane, Bloch-Zupan, Agnès, Klein, Ophir D., Viriot, Laurent

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A possible cranio-oro-facial phenotype in Cockayne syndrome by Bloch-Zupan, Agnès, Rousseaux, Morgan, Laugel, Virginie, Schmittbuhl, Matthieu, Mathis, Rémy, Desforges, Emmanuelle, Koob, Mériam, Zaloszyc, Ariane, Dollfus, Hélène, Laugel, Vincent

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Enamel and dental anomalies in latent‐transforming growth factor beta‐binding protein 3 mutant mice by Morkmued, Supawich, Hemmerle, Joseph, Mathieu, Eric, Laugel‐Haushalter, Virginie, Dabovic, Branka, Rifkin, Daniel B., Dollé, Pascal, Niederreither, Karen, Bloch‐Zupan, Agnès

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A Novel Mutation in the ROGDI Gene in a Patient with Kohlschütter-Tönz Syndrome by Huckert, Mathilde, Mecili, Helen, Laugel-Haushalter, Virginie, Stoetzel, Corinne, Muller, Jean, Flori, Elisabeth, Laugel, Vincent, Manière, Marie-Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès

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COVID-19 and Dentistry in 72 Questions: An Overview of the Literature by Derruau, Stéphane, Bouchet, Jérôme, Nassif, Ali, Baudet, Alexandre, Yasukawa, Kazutoyo, Lorimier, Sandrine, Prêcheur, Isabelle, Bloch-Zupan, Agnès, Pellat, Bernard, Chardin, Hélène, Jung, Sophie

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Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss by Morkmued, Supawich, Clauss, François, Schuhbaur, Brigitte, Fraulob, Valérie, Mathieu, Eric, Hemmerlé, Joseph, Clevers, Hans, Koo, Bon-Kyoung, Dollé, Pascal, Bloch-Zupan, Agnès, Niederreither, Karen

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Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations by de la Dure-Molla, Muriel, Quentric, Mickael, Yamaguti, Paulo Marcio, Acevedo, Ana-Carolina, Mighell, Alan J, Vikkula, Miikka, Huckert, Mathilde, Berdal, Ariane, Bloch-Zupan, Agnes

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Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects by Bloch-Zupan, Agnès, Jamet, Xavier, Etard, Christelle, Laugel, Virginie, Muller, Jean, Geoffroy, Véronique, Strauss, Jean-Pierre, Pelletier, Valérie, Marion, Vincent, Poch, Olivier, Strahle, Uwe, Stoetzel, Corinne, Dollfus, Hélène

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning by Laugel-Haushalter, Virginie, Morkmued, Supawich, Stoetzel, Corinne, Geoffroy, Véronique, Muller, Jean, Boland, Anne, Deleuze, Jean-François, Chennen, Kirsley, Pitiphat, Waranuch, Dollfus, Hélène, Niederreither, Karen, Bloch-Zupan, Agnès, Pungchanchaikul, Patimaporn

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Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta by Gasse, Barbara, Prasad, Megana, Delgado, Sidney, Huckert, Mathilde, Kawczynski, Marzena, Garret-Bernardin, Annelyse, Lopez-Cazaux, Serena, Bailleul-Forestier, Isabelle, Manière, Marie-Cécile, Stoetzel, Corinne, Bloch-Zupan, Agnès, Sire, Jean-Yves

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A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta by Laugel-Haushalter, Virginie, Bär, Séverine, Schaefer, Elise, Stoetzel, Corinne, Geoffroy, Véronique, Alembik, Yves, Kharouf, Naji, Huckert, Mathilde, Hamm, Pauline, Hemmerlé, Joseph, Manière, Marie-Cécile, Friant, Sylvie, Dollfus, Hélène, Bloch-Zupan, Agnès

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RSK2 Is a Modulator of Craniofacial Development by Laugel-Haushalter, Virginie, Paschaki, Marie, Marangoni, Pauline, Pilgram, Coralie, Langer, Arnaud, Kuntz, Thibaut, Demassue, Julie, Morkmued, Supawich, Choquet, Philippe, Constantinesco, André, Bornert, Fabien, Schmittbuhl, Matthieu, Pannetier, Solange, Viriot, Laurent, Hanauer, André, Dollé, Pascal, Bloch-Zupan, Agnès

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