Ohcanbohtosat - Netchine, Irène

SAT-039 GNAS-miRNAs Are Likely Involved in the Phenotype of Patients with Pseudohypoparathyroidism 1B/iPPSD3 Dahkki Hanna, Patrick, Netchine, Irène, Le Stunff, Catherine, Linglart, Agnès

Viečča ollesdeavstta Viečča ollesdeavstta

IGF2: Development, Genetic and Epigenetic Abnormalities Dahkki Sélénou, Céline, Brioude, Frédéric, Giabicani, Eloïse, Sobrier, Marie-Laure, Netchine, Irène

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Human 3beta-hydroxysteroid dehydrogenase deficiency associated with normal spermatic numeration despite a severe enzyme deficit Dahkki Donadille, Bruno, Houang, Muriel, Netchine, Irène, Siffroi, Jean-Pierre, Christin-Maitre, Sophie

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

New Horizons in Short Children Born Small for Gestational Age Dahkki Netchine, Irène, van der Steen, Manouk, López-Bermejo, Abel, Koledova, Ekaterina, Maghnie, Mohamad

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Dysgenesis of the Internal Carotid ArteryAssociated with Transsphenoidal Encephalocele:A Neural Crest Syndrome? Dahkki Blustajn, Jerry, Netchine, Irène, Frédy, Daniel, Bakouche, Pierre, Piekarski, Jean Daniel, Meder, Jean François

Viečča ollesdeavstta Viečča ollesdeavstta

Roles of Type 1 Insulin-Like Growth Factor (IGF) Receptor and IGF-II in Growth Regulation: Evidence From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion Dahkki Giabicani, Eloïse, Chantot-Bastaraud, Sandra, Bonnard, Adeline, Rachid, Myriam, Whalen, Sandra, Netchine, Irène, Brioude, Frédéric

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome Dahkki Azzi, Salah, Salem, Jennifer, Thibaud, Nathalie, Chantot-Bastaraud, Sandra, Lieber, Eli, Netchine, Irène, Harbison, Madeleine D

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants Dahkki Pham, Aurélie, Sobrier, Marie-Laure, Giabicani, Eloïse, Le Jules Fernandes, Marilyne, Mitanchez, Delphine, Brioude, Fréderic, Netchine, Irène

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Analysis of a pitfall in congenital adrenal hyperplasia newborn screening: evidence of maternal use of corticoids detected on dried blood spot Dahkki Houang, Muriel, Nguyen-Khoa, Thao, Eguether, Thibaut, Ribault, Bettina, Brabant, Séverine, Polak, Michel, Netchine, Irène, Lamazière, Antonin

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network Dahkki Eggermann, Thomas, Davies, Justin H., Tauber, Maithé, van den Akker, Erica, Hokken-Koelega, Anita, Johansson, Gudmundur, Netchine, Irène

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction Dahkki Chantot-Bastaraud, Sandra, Stratmann, Svea, Brioude, Frédéric, Begemann, Matthias, Elbracht, Miriam, Graul-Neumann, Luitgard, Harbison, Madeleine, Netchine, Irène, Eggermann, Thomas

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth Dahkki Pham, Aurelie, Mitanchez, Delphine, Forhan, Anne, Perin, Laurence, Le Bouc, Yves, Brioude, Frederic, Sobrier, Marie-Laure, Heude, Barbara, Netchine, Irene

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Degree of methylation of ZAC1 (PLAGL1) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort Dahkki Azzi, Salah, Sas, Theo CJ, Koudou, Yves, Le Bouc, Yves, Souberbielle, Jean-Claude, Dargent-Molina, Patricia, Netchine, Irène, Charles, Marie-Aline

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Dental pulp stem cells as a promising model to study imprinting diseases Dahkki Giabicani, Eloïse, Pham, Aurélie, Sélénou, Céline, Sobrier, Marie-Laure, Andrique, Caroline, Lesieur, Julie, Linglart, Agnès, Poliard, Anne, Chaussain, Catherine, Netchine, Irène

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical care Dahkki Eggermann, Thomas, Netchine, Irène, Temple, I Karen, Tümer, Zeynep, Monk, David, Mackay, Deborah, Grønskov, Karin, Riccio, Andrea, Linglart, Agnès, Maher, Eamonn R

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Clinical utility gene card for: Beckwith–Wiedemann Syndrome Dahkki Eggermann, Thomas, Algar, Elizabeth, Lapunzina, Pablo, Mackay, Deborah, Maher, Eamonn R, Mannens, Marcel, Netchine, Irène, Prawitt, Dirk, Riccio, Andrea, Temple, I Karen, Weksberg, Rosanna

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development Dahkki Netchine, Irène, Azzi, Salah, Houang, Muriel, Seurin, Danielle, Perin, Laurence, Ricort, Jean-Marc, Daubas, Claudine, Legay, Christine, Mester, Jan, Herich, Robert, Godeau, François, Le Bouc, Yves

Viečča ollesdeavstta Viečča ollesdeavstta

Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders Dahkki Abi Habib, Walid, Brioude, Frédéric, Azzi, Salah, Rossignol, Sylvie, Linglart, Agnès, Sobrier, Marie-Laure, Giabicani, Éloïse, Steunou, Virginie, Harbison, Madeleine D., Le Bouc, Yves, Netchine, Irène

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Syndromic Short Stature in Patients with a Germline Mutation in the LIM Homeobox LHX4 Dahkki Machinis, Kalotina, Pantel, Jacques, Netchine, Irène, Léger, Juliane, Camand, Olivier J. A., Sobrier, Marie-Laure, Moal, Florence Dastot-Le, Duquesnoy, Philippe, Abitbol, Marc, Czernichow, Paul, Amselem, Serge

Viečča ollesdeavstta Viečča ollesdeavstta

Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci Dahkki Eggermann, Thomas, de Nanclares, Guiomar Perez, Maher, Eamonn R., Temple, I. Karen, Tümer, Zeynep, Monk, David, Mackay, Deborah J. G., Grønskov, Karen, Riccio, Andrea, Linglart, Agnès, Netchine, Irène

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta