Otodental syndrome

por Bloch-Zupan, Agnès, Goodman, Jane R
Publicado 2006

Amelogenesis imperfecta

por Crawford, Peter JM, Aldred, Michael, Bloch-Zupan, Agnes
Publicado 2007

Primary failure of eruption: From molecular diagnosis to therapeutic management

por Wagner, Delphine, Rey, Tristan, Maniere, Marie-Cécile, Dubourg, Sarah, Bloch-Zupan, Agnès, Strub, Marion
Publicado 2023

Molars and incisors: show your microarray IDs

por Laugel-Haushalter, Virginie, Paschaki, Marie, Thibault-Carpentier, Christelle, Dembelé, Doulaye, Dollé, Pascal, Bloch-Zupan, Agnès
Publicado 2013

Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review

por Hejlesen, Jane, Underbjerg, Line, Gjørup, Hans, Bloch-Zupan, Agnes, Sikjaer, Tanja, Rejnmark, Lars, Haubek, Dorte
Publicado 2018

Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

por Reibel, Amélie, Manière, Marie-Cécile, Clauss, François, Droz, Dominique, Alembik, Yves, Mornet, Etienne, Bloch-Zupan, Agnès
Publicado 2009

Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects

por Morkmued, Supawich, Laugel-Haushalter, Virginie, Mathieu, Eric, Schuhbaur, Brigitte, Hemmerlé, Joseph, Dollé, Pascal, Bloch-Zupan, Agnès, Niederreither, Karen
Publicado 2017

Phenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a model

por Marangoni, Pauline, Charles, Cyril, Tafforeau, Paul, Laugel-Haushalter, Virginie, Joo, Adriane, Bloch-Zupan, Agnès, Klein, Ophir D., Viriot, Laurent
Publicado 2015

A possible cranio-oro-facial phenotype in Cockayne syndrome

por Bloch-Zupan, Agnès, Rousseaux, Morgan, Laugel, Virginie, Schmittbuhl, Matthieu, Mathis, Rémy, Desforges, Emmanuelle, Koob, Mériam, Zaloszyc, Ariane, Dollfus, Hélène, Laugel, Vincent
Publicado 2013

Enamel and dental anomalies in latent‐transforming growth factor beta‐binding protein 3 mutant mice

por Morkmued, Supawich, Hemmerle, Joseph, Mathieu, Eric, Laugel‐Haushalter, Virginie, Dabovic, Branka, Rifkin, Daniel B., Dollé, Pascal, Niederreither, Karen, Bloch‐Zupan, Agnès
Publicado 2017

COVID-19 and Dentistry in 72 Questions: An Overview of the Literature

por Derruau, Stéphane, Bouchet, Jérôme, Nassif, Ali, Baudet, Alexandre, Yasukawa, Kazutoyo, Lorimier, Sandrine, Prêcheur, Isabelle, Bloch-Zupan, Agnès, Pellat, Bernard, Chardin, Hélène, Jung, Sophie
Publicado 2021

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss

por Morkmued, Supawich, Clauss, François, Schuhbaur, Brigitte, Fraulob, Valérie, Mathieu, Eric, Hemmerlé, Joseph, Clevers, Hans, Koo, Bon-Kyoung, Dollé, Pascal, Bloch-Zupan, Agnès, Niederreither, Karen
Publicado 2020

Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations

por 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
Publicado 2014

Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning

por 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
Publicado 2018

Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta

por 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
Publicado 2017

A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta

por 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
Publicado 2019

RSK2 Is a Modulator of Craniofacial Development

por 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
Publicado 2014

Hypomorphic mutations of TRIP11 cause odontochondrodysplasia

por Wehrle, Anika, Witkos, Tomasz M., Unger, Sheila, Schneider, Judith, Follit, John A., Hermann, Johannes, Welting, Tim, Fano, Virginia, Hietala, Marja, Vatanavicharn, Nithiwat, Schoner, Katharina, Spranger, Jürgen, Schmidts, Miriam, Zabel, Bernhard, Pazour, Gregory J., Bloch-Zupan, Agnes, Nishimura, Gen, Superti-Furga, Andrea, Lowe, Martin, Lausch, Ekkehart
Publicado 2019

Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar

por Bloch-Zupan, Agnès, Huckert, Mathilde, Stoetzel, Corinne, Meyer, Julia, Geoffroy, Véronique, Razafindrakoto, Rabisoa W., Ralison, Saholy N., Randrianaivo, Jean-Claude, Ralison, Georgette, Andriamasinoro, Rija O., Ramanampamaharana, Rija H., Randrianazary, Solofomanantsoa E., Ralimanana, Louise H., Richard, Béatrice, Gorry, Philippe, Manière, Marie-Cécile, Rasoamananjara, Jeanne A., Rakoto Alson, Simone, Dollfus, Hélène
Publicado 2016

Corrigendum: Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar

por Bloch-Zupan, Agnès, Huckert, Mathilde, Stoetzel, Corinne, Meyer, Julia, Geoffroy, Véronique, Razafindrakoto, Rabisoa W., Ralison, Saholy N., Randrianaivo, Jean-Claude, Ralison, Georgette, Andriamasinoro, Rija O., Ramanampamaharana, Rija H., Randrianazary, Solofomanantsoa E., Ralimanana, Louise H., Richard, Béatrice, Gorry, Philippe, Manière, Marie-Cécile, Rasoamananjara, Jeanne A., Rakoto Alson, Simone, Dollfus, Hélène
Publicado 2016