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Lung disease modifier genes in cystic fibrosis.
Guillot L, Beucher J, Tabary O, Le Rouzic P, Clement A, Corvol H. Guillot L, et al. Among authors: beucher j. Int J Biochem Cell Biol. 2014 Jul;52:83-93. doi: 10.1016/j.biocel.2014.02.011. Epub 2014 Feb 22. Int J Biochem Cell Biol. 2014. PMID: 24569122 Review.
[Genetics and modifier genes, atypical and rare forms].
Férec C, Scotet V, Beucher J, Corvol H. Férec C, et al. Among authors: beucher j. Arch Pediatr. 2012 May;19 Suppl 1:S3-7. doi: 10.1016/S0929-693X(12)71099-0. Arch Pediatr. 2012. PMID: 22682487 Review. French.
Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients.
Corvol H, Beucher J, Boëlle PY, Busson PF, Muselet-Charlier C, Clement A, Ratjen F, Grasemann H, Laki J, Palmer CN, Elborn JS, Mehta A. Corvol H, et al. Among authors: beucher j. J Cyst Fibros. 2012 Jan;11(1):63-7. doi: 10.1016/j.jcf.2011.09.006. Epub 2011 Oct 10. J Cyst Fibros. 2012. PMID: 21993476 Free article.
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.
Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, Just J, Nathan N, Tamalet A, Collot N, Jeanson L, Le Gouez M, Vallette B, Vojtek AM, Epaud R, Coste A, Clement A, Housset B, Louis B, Escudier E, Amselem S. Kott E, et al. Among authors: beucher j. Am J Hum Genet. 2013 Sep 5;93(3):561-70. doi: 10.1016/j.ajhg.2013.07.013. Epub 2013 Aug 29. Am J Hum Genet. 2013. PMID: 23993197 Free PMC article.
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