%0
Generic
%T
A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype
%A Terhal, Paulien A.
%A Nievelstein, Rutger Jan A. J.
%A Verver, Eva J. J.
%A Topsakal, Vedat
%A van Dommelen, Paula
%A Hoornaert, Kristien
%A Le Merrer, Martine
%A Zankl, Andreas
%A Simon, Marleen E. H.
%A Smithson, Sarah F.
%A Marcelis, Carlo
%A Kerr, Bronwyn
%A Clayton‐Smith, Jill
%A Kinning, Esther
%A Mansour, Sahar
%A Elmslie, Frances
%A Goodwin, Linda
%A van der Hout, Annemarie H.
%A Veenstra‐Knol, Hermine E.
%A Herkert, Johanna C.
%A Lund, Allan M.
%A Hennekam, Raoul C. M.
%A Mégarbané, André
%A Lees, Melissa M.
%A Wilson, Louise C.
%A Male, Alison
%A Hurst, Jane
%A Alanay, Yasemin
%A Annerén, Göran
%A Betz, Regina C.
%A Bongers, Ernie M. H. F.
%A Cormier‐Daire, Valerie
%A Dieux, Anne
%A David, Albert
%A Elting, Mariet W.
%A van den Ende, Jenneke
%A Green, Andrew
%A van Hagen, Johanna M.
%A Hertel, Niels Thomas
%A Holder‐Espinasse, Muriel
%A den Hollander, Nicolette
%A Homfray, Tessa
%A Hove, Hanne D.
%A Price, Susan
%A Raas‐Rothschild, Annick
%A Rohrbach, Marianne
%A Schroeter, Barbara
%A Suri, Mohnish
%A Thompson, Elizabeth M.
%A Tobias, Edward S.
%A Toutain, Annick
%A Vreeburg, Maaike
%A Wakeling, Emma
%A Knoers, Nine V.
%A Coucke, Paul
%A Mortier, Geert R.
%I Wiley
%@ 1552-4825
%@ 1552-4833
%D 2015
%C Wiley
%U http://slubdd.de/katalog?TN_libero_mab2