| Literature DB >> 7923865 |
E Smeets1, J P Fryns, H Van den Berghe.
Abstract
In this report we describe a 26-year-old female with the typical clinical symptoms and signs of Melkersson-Rosenthal syndrome, an autosomal dominant with variable expression, and a de novo t(9;21)(p11;p11), and suggest that the "Melkersson-Rosenthal gene" is located at 9p11.Entities:
Mesh:
Year: 1994 PMID: 7923865 DOI: 10.1111/j.1399-0004.1994.tb04041.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438