| Literature DB >> 7554347 |
J M Hertz1, N Tommerup, F B Sørensen, U V Henriques, A Nielsen, A J Therkelsen.
Abstract
We describe the cytogenetic findings and the dysmorphic features in a stillborn girl with a large de novo terminal deletion of the long arm of chromosome 11. The karyotype was 46,XX,del(11)(q21qter). By reviewing previous reports of deletion 11q, we found that cleft lip and palate are most frequently seen in proximal 11q deletions involving 11q21. Telomeric staining using the PRINS technique demonstrated normal telomeric sequences in the deleted chromosome 11.Entities:
Mesh:
Year: 1995 PMID: 7554347 DOI: 10.1111/j.1399-0004.1995.tb04302.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438