Mapping of hereditary trichilemmal cyst(TRICY1)to chromosome 3p24-p21.2 and exclusion of β-CATENINandMLH1-Reference-Cited by-同舟云学术

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Mapping of hereditary trichilemmal cyst(TRICY1)to chromosome 3p24-p21.2 and exclusion of β-CATENINandMLH1

Published:2005-01-06 Issue:1 Volume:133A Page:44-47
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Eiberg Hans,Hansen Lars,Hansen Claus,Mohr Jan,Teglbjaerg Peter Stubbe,Kjaer Klaus Wilbrandt

Funder

Danish Medical Research Council

Danish National Research Foundation

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. The genetic basis of Muir-Torre syndrome includes the hMLH1 locus;Bapat;Am J Hum Genet,1996

2. A common human skin tumour is caused by activating mutations in beta-catenin;Chan;Nat Genet,1999

3. A comprehensive genetic map of the human genome based on 5,264 microsatellites;Dib;Nature,1996

4. Linkage between serum cholinesterase 2 (CHE2) and gamma-crystalline gene cluster (CRYG): Assignment to chromosome 2;Eiberg;Clin Genet,1989

5. Assignment of granular corneal dystrophy Groenouw type I (CDGG1) to chromosome 5q. Close linkage to IL9, D5S210 and D5S119;Eiberg;Eur J Human Genet,1994

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