FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum
Reuter, Miriam S, Riess, Angelika, Moog, Ute, Briggs, Tracy A, Chandler, Kate E, Rauch, Anita, Stampfer, Miriam, Steindl, Katharina, Gläser, Dieter, Joset, Pascal, Krumbiegel, Mandy, Rabe, Harald, Schulte-Mattler, Uta, Bauer, Peter, Beck-Wödl, Stefanie, Kohlhase, Jürgen, Reis, André, Zweier, Christiane
Published in Journal of medical genetics (01.01.2017)
Published in Journal of medical genetics (01.01.2017)
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Journal Article
9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardationand tic
ZWEIER, Christiane, GUTH, Sabine, SCHULTE-MATTLER, Uta, RAUCH, Anita, TRAUTMANN, Udo
Published in European journal of medical genetics (2005)
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Published in European journal of medical genetics (2005)
Journal Article
9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and tic
Zweier, Christiane, Guth, Sabine, Schulte-Mattler, Uta, Rauch, Anita, Trautmann, Udo
Published in European journal of medical genetics (01.07.2005)
Published in European journal of medical genetics (01.07.2005)
Get full text
Journal Article
9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and tic
Zweier, Christiane, Guth, Sabine, Schulte-Mattler, Uta, Rauch, Anita, Trautmann, Udo
Published in European journal of medical genetics (01.07.2005)
Get full text
Published in European journal of medical genetics (01.07.2005)
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