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Partial deletion 11q: report of a case with a large terminal deletion 11q21-qter without loss of telomeric sequences, and review of the literature.

作者信息

Hertz J M, Tommerup N, Sørensen F B, Henriques U V, Nielsen A, Therkelsen A J

机构信息

Institute of Human Genetics, University of Aarhus, Denmark.

出版信息

Clin Genet. 1995 May;47(5):231-5. doi: 10.1111/j.1399-0004.1995.tb04302.x.

DOI:10.1111/j.1399-0004.1995.tb04302.x
PMID:7554347
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.

摘要

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