| Literature DB >> 11173835 |
A Dufke1, J Seidel, M Schöning, M Döbler-Neumann, C Kelbova, T Liehr, V Beensen, C Backsch, U Klein-Vogler, H Enders.
Abstract
Wolf-Hirschhorn syndrome (WHS) is a multiple malformation syndrome caused by partial monosomy of 4p16.3. Pitt-Rogers-Danks syndrome, first thought to be a distinct entity, is a similar condition associated with a microdeletion overlapping the WHS critical region. In this paper we evaluate three WHS patients showing a microdeletion of 4p and remarkable development with respect to the clinical spectrum of WHS. Copyright 2001 S. Karger AG, BaselEntities:
Mesh:
Year: 2000 PMID: 11173835 DOI: 10.1159/000056823
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171