Am J Med Genet. 1991 Sep 1;40(3):343-4.

Apparent late-onset Cockayne syndrome and interstitial deletion of the long arm of chromosome 10 (del(10)(q11.23q21.2)).

Fryns JP, Bulcke J, Verdu P, Carton H, Kleczkowska A, Van den Berghe H.

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Center for Human Genetics, University of Leuven, Belgium.

Abstract

We present the history and data on a 24-year-old man with clinical and neurological symptoms similar to the findings in patients with late-onset Cockayne syndrome. Prometaphase chromosome studies documented an interstitial 10q211 deletion in all cells. This finding may indicate that the gene for late Cockayne syndrome is at 10q211.

PMID:: 1951442; [PubMed - indexed for MEDLINE]

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Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21). [Am J Med Genet. 1985]
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Cited by 3 PubMed Central articles

Review Cockayne syndrome in adults: review with clinical and pathologic study of a new case. [J Child Neurol. 2006]
Review Cockayne syndrome in adults: review with clinical and pathologic study of a new case.
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The many faces of Cockayne syndrome. [Proc Natl Acad Sci U S A. 2004]
The many faces of Cockayne syndrome.
Spivak G. Proc Natl Acad Sci U S A. 2004 Oct 26; 101(43):15273-4. Epub 2004 Oct 19.
Review Interstitial deletion of chromosome 10q23: a new case and review. [J Med Genet. 1993]
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