A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
Autor: | Seidel, Jörg1 joerg.seidel@med.uni-jena.de, Heller, Anita2, Senger, Gabriele3, Starke, Heike2, Chudoba, Ilse4, Kelbova, Christina5, Tönnies, Holger6, Neitzel, Heidemarie6, Haase, Claudia1, Beensen, Volkmar2, Zintl, Felix1, Claussen, Uwe2, Liehr, Thomas2, Seidel, Jörg7 (AUTHOR), Tönnies, Holger (AUTHOR) |
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Zdroj: | European Journal of Pediatrics. 2003, Vol. 162 Issue 9, p582-588. 7p. |
Databáze: | Academic Search Ultimate |
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