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

✍ Scribed by Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christina Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr

• Publisher: Springer
• Year: 2003
• Tongue: English
• Weight: 933 KB
• Volume: 162
• Category: Article
• ISSN: 0340-6997
• DOI: 10.1007/s00431-003-1254-3