bobler_bla2

Greinar 2011-2013

Gronskov K, Dooley C. M, Ostergaard E., Kelsh R. N., Hansen L., Levesque M. P, Vilhelmsen, K Møllgård K, Stemple D.L, Rosenberg T
Mutations in C10orf11, encoding a melanocyte differentiation gene, cause autosomal recessive Albinism. Am J Hum Genet. 2013 Mar 7;92(3):415-21. doi: 10.1016/j.ajhg.2013.01.006. Epub 2013 Feb 7.

Gal A, Rau I, El ML, et al. 
Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease. Am J Hum Genet 2011;88:382-90.

Ostergaard E, Duno M, Batbayli M, et al. 
A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases. Mol Vis 2011;17:1485-92.

Joensen, P. 
Incidence of amyotrophic lateral sclerosis in the Faroe Islands. Acta Neurol Scand. 2012 Jul;126(1):62-6. doi: 10.1111/j.1600-0404.2011.01611.x. Epub 2011 Oct 29.

Joensen P.

Multiple sclerosis: variation of incidence of onset over time in the Faroe Islands.
Mult Scler. 2011 Aug 26. No abstract available. PMID:21873517 

Joensen P. 
Multiple sclerosis: variation of incidence of onset over time in the Faroe Islands. Mult Scler. 2011


 
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