Literature DB >> 7554347

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

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.

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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


  3 in total

1.  At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Authors:  D Smeets; C van Ravenswaaij; J de Pater; K Gerssen-Schoorl; J Van Hemel; G Janssen; A Smits
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

Review 2.  Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Authors:  E K Pivnick; G V Velagaleti; R S Wilroy; M E Smith; S R Rose; R E Tipton; A T Tharapel
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

3.  Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report.

Authors:  Danijela Krgovic; Natasa Marcun Varda; Andreja Zagorac; Nadja Kokalj-Vokac
Journal:  Mol Cytogenet       Date:  2011-08-22       Impact factor: 2.009

  3 in total

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