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SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
Am J Hum Genet. 2008 Apr;82(4):1003-10. doi: 10.1016/j.ajhg.2008.01.013. Epub 2008 Mar 13.
Am J Hum Genet. 2008.
PMID: 18342287
Free PMC article.
Friedreich ataxia in Norway - an epidemiological, molecular and clinical study.
Wedding IM, Kroken M, Henriksen SP, Selmer KK, Fiskerstrand T, Knappskog PM, Berge T, Tallaksen CM.
Wedding IM, et al. Among authors: kroken m.
Orphanet J Rare Dis. 2015 Sep 4;10:108. doi: 10.1186/s13023-015-0328-4.
Orphanet J Rare Dis. 2015.
PMID: 26338206
Free PMC article.
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Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1.
Heimdal K, Dalhus B, Rødningen OK, Kroken M, Eiklid K, Dheyauldeen S, Røysland T, Andersen R, Kulseth MA.
Heimdal K, et al. Among authors: kroken m.
Clin Genet. 2016 Feb;89(2):182-6. doi: 10.1111/cge.12612. Epub 2015 Jun 5.
Clin Genet. 2016.
PMID: 25970827
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Temple syndrome as a differential diagnosis to Prader-Willi syndrome: Identifying three new patients.
Lande A, Kroken M, Rabben K, Retterstøl L.
Lande A, et al. Among authors: kroken m.
Am J Med Genet A. 2018 Jan;176(1):175-180. doi: 10.1002/ajmg.a.38533. Epub 2017 Nov 21.
Am J Med Genet A. 2018.
PMID: 29159982
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Variations in fetal phenotype in Prader-Willi syndrome.
Haugen G, Rønnestad A, Kroken M.
Haugen G, et al. Among authors: kroken m.
Prenat Diagn. 2009 Mar;29(3):294. doi: 10.1002/pd.2207.
Prenat Diagn. 2009.
PMID: 19248040
No abstract available.
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Rapid, universal method to isolate PCR-ready DNA using magnetic beads.
Rudi K, Kroken M, Dahlberg OJ, Deggerdal A, Jakobsen KS, Larsen F.
Rudi K, et al. Among authors: kroken m.
Biotechniques. 1997 Mar;22(3):506-11. doi: 10.2144/97223rr01.
Biotechniques. 1997.
PMID: 9067030
Free article.
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