Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus
- Creator: Sy, Mary R. , Chauhan, Jaynee , Islam, Lily , Goel, Himanshu , Bain, Nicole , Park, Soo-Mi , Mohammed, Shehla , Dieterich, Klaus , Coutton, Charles , Satre, Veronique , Vieville, Gaelle , Donaldson, Alan , Prescott, Katrina , Beneteau, C , Ghoumid, J , Van den Bogaert, K , Boogaerts, A , Boudry, E , Vanlerberghe, C , Petit, F , Bernardini, L , Torres, B , Mattina, T , Imam, Aliza , Carli, D , Mandrile, G , Pinelli, M , Brunetti-Pierri, N , Neas, K , Beddow, R , Torring, PM , Faletra, F , Spedicati, B , Gasparini, P , Kraus, Alison , Mussa, A , Ferrero, GB , Lampe, A , Lam, W , Bi, W , Bacino, CA , Kuwahara, A , Bush, JO , Zhao, X , Luna, PN , Beleza, Ana , Shaw, CA , Rosenfeld, JA , Scott, DA , Salkeld, Lee , Hosdurga, Saraswati , Parker, Michael , Vasudevan, Pradeep
- Resource Type: journal article
- Date: 2022
FOXP1 mutations cause intellectual disability and a recognizable phenotype
- Creator: Le Fevre, Anna K. , Taylor, Sharelle , Bain, Nicole , Fagan, Kerry , Hunter, Matthew F. , Malek, Neva H. , Horn, Denise , Carr, Christopher W. , Abdul-Rahman, Omar A. , O'Donnell, Sherindan , Burgess, Trent , Shaw, Marie , Gecz, Jozef
- Resource Type: journal article
- Date: 2013