Authors: Sen, Partha, Yang, Yaping, Navarro, Colby, Silva, Iris, Szafranski, Przemyslaw, Kolodziejska, Katarzyna E, Dharmadhikari, Avinash V, Mostafa, Hasnaa, Kozakewich, Harry, Kearney, Debra, Cahill, John B, Whitt, Merrissa, Bilic, Masha, Margraf, Linda, Charles, Adrian, Goldblatt, Jack, Gibson, Kathleen, Lantz, Patrick E, Garvin, A Julian, Petty, John, Kiblawi, Zeina, Zuppan, Craig, McConkie-Rosell, Allyn, McDonald, Marie T, Peterson-Carmichael, Stacey L, Gaede, Jane T, Shivanna, Binoy, Schady, Deborah, Friedlich, Philippe S, Hays, Stephen R, Palafoll, Irene Valenzuela, Siebers-Renelt, Ulrike, Bohring, Axel, Finn, Laura S, Siebert, Joseph R, Galambos, Csaba, Nguyen, Lananh, Riley, Melissa, Chassaing, Nicolas, Vigouroux, Adeline, Rocha, Gustavo, Fernandes, Susana, Brumbaugh, Jane, Roberts, Kari, Ho-Ming, Luk, Lo, Ivan F M, Lam, Stephen, Gerychova, Romana, Jezova, Marta, Valaskova, Iveta, Fellmann, Florence, Afshar, Katayoun, Giannoni, Eric, Muhlethaler, Vincent, Liang, Jinlong, Beckmann, Jacques S, Lioy, Janet, Deshmukh, Hitesh, Srinivasan, Lakshmi, Swarr, Daniel T, Sloman, Melissa, Shaw-Smith, Charles, van Loon, Rosa Laura, Hagman, Cecilia, Sznajer, Yves, Barréa, Catherine, Galant, Christine, Detaille, Thierry, Wambach, Jennifer A, Cole, F Sessions, Hamvas, Aaron, Prince, Lawrence S, Diderich, Karin E M, Brooks, Alice S, Verdijk, Robert M, Ravindranathan, Hari, Sugo, Ella, Mowat, David, Baker, Michael L, Langston, Claire, Welty, Stephen, Stankiewicz, Pawel
Contributors: UCL - SSS/IREC - Institut de recherche expérimentale et clinique, UCL - SSS/IREC/MORF - Pôle de Morphologie, UCL - SSS/IREC/PEDI - Pôle de Pédiatrie, UCL - (SLuc) Service d'anatomie pathologique, UCL - (SLuc) Centre de génétique médicale UCL, UCL - (SLuc) Service de cardiologie pédiatrique, UCL - (SLuc) Service de soins intensifs
Superior Title: Human Mutation, Vol. 34, no. 6, p. 801-811 (2013)
Subject Terms: Amino Acid Sequence, Infant, Newborn, Male, Molecular Sequence Data, Mutation, Open Reading Frames, Persistent Fetal Circulation Syndrome, Protein Interaction Domains and Motifs, Sequence Alignment, Chromosome Mapping, Databases, Genetic, Female, Forkhead Transcription Factors, Gene Dosage, Gene Order, Humans
Relation: boreal:151866; http://hdl.handle.net/2078.1/151866; info:pmid/23505205; urn:ISSN:1059-7794; urn:EISSN:1098-1004
