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Journal Article
Horn, Denise, Kapeller, Johannes, Rivera-Brugues, Nria, Moog, Ute, Lorenz-Depiereux, Bettina, Eck, Sebastian, Hempel, Maja, Wagenstaller, Janine, Gawthrope, Alex, Monaco, Anthony P., Bonin, Michael, Riess, Olaf, Wohlleber, Eva, Illig, Thomas, Bezzina, Connie R., Franke, Andre 
ORCID: 0000-0003-1530-5811, Spranger, Stephanie, Villavicencio-Lorini, Pablo, Seifert, Wenke, Rosenfeld, Jochen, Klopocki, Eva ORCID: 0000-0003-1438-2081, Rappold, Gudrun A. and Strom, Tim M.
(2010).
Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits.
Hum. Mutat., 31 (11).
S. E1851 - 10.
MALDEN:
WILEY-BLACKWELL.
ISSN 1059-7794
Montalbano, Antonino, Juergensen, Lonny, Roeth, Ralph, Weiss, Birgit, Fukami, Maki ORCID: 0000-0001-9971-4035, Fricke-Otto, Susanne, Binder, Gerhard, Ogata, Tsutomu ORCID: 0000-0001-7178-9991, Decker, Eva, Nuernberg, Gudrun, Hassel, David and Rappold, Gudrun A.
(2016).
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.
EMBO Mol. Med., 8 (12).
S. 1455 - 1470.
HOBOKEN:
WILEY.
ISSN 1757-4684