Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndrome-Reference-Cited by-同舟云学术

Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndrome

Published:2004-02-18 Issue:5 Volume:12 Page:415-418
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Meur Nathalie Le,Martin Cosette,Saugier-Veber Pascale,Joly Géraldine,Lemoine Françoise,Moirot Hélène,Rossi Annick,Bachy Bruno,Cabot Annick,Joly Pascal,Frébourg Thierry

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201155.pdf

Reference23 articles.

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5. Hemminki A, Tomlinson I, Markie D et al: Localization of a susceptibility locus for Peutz–Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. Nat Genet 1997; 15: 87–90.

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