| Literature DB >> 3960564 |
J Sigmund, H Frisch, P Heinz-Erian, K Rhomberg, R D Wegner.
Abstract
A partial monosomy 5p leading to the Cri du chat-Syndrome combined with a partial trisomy 9p was observed in a mentally defective boy with typical clinical features for both syndromes. This chromosomal aberration is inherited from a t [5; 9] (p. 13.3; 13.1) translocation carrier father. Further family investigations showed many balanced translocation carriers through several generations.Entities:
Mesh:
Year: 1986 PMID: 3960564
Source DB: PubMed Journal: Padiatr Padol ISSN: 0030-9338