| Literature DB >> 11310998 |
E Petek, G Köstl, L Rauter, I Mutz, K Wagner, P M Kroisel.
Abstract
The molecular-cytogenetic characterization of a de novo pure partial trisomy 10(q24.33-qter) is described. This report provides information about the postnatal phenotype. The clinical findings observed in this case support the conclusion that the more severe disease related genes are located between 10q24.1 and q24.33.Mesh:
Year: 2001 PMID: 11310998 DOI: 10.1097/00019605-200104000-00015
Source DB: PubMed Journal: Clin Dysmorphol ISSN: 0962-8827 Impact factor: 0.816