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Journal Article

Hagen, Anja, Bigl, Arndt, Wand, Dorothea, Klopocki, Eva ORCID: 0000-0003-1438-2081, Heller, Raoul, Siekmeyer, Manuela, Siekmeyer, Werner, Kiess, Wieland and Merkenschlager, Andreas (2011). Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: Phenotypic and genotypic findings. Am. J. Med. Genet. A, 155A (12). S. 3075 - 3082. MALDEN: WILEY-BLACKWELL. ISSN 1552-4825

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

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