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Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease.
Nørremølle A, Sørensen SA, Fenger K, Hasholt L. Nørremølle A, et al. Among authors: fenger k. Clin Genet. 1995 Mar;47(3):113-7. doi: 10.1111/j.1399-0004.1995.tb03941.x. Clin Genet. 1995. PMID: 7634532
PEDIGREE-PLOT: a computer program for plotting pedigrees.
Fenger K, Sørensen SA. Fenger K, et al. Clin Genet. 1987 Oct;32(4):284-6. doi: 10.1111/j.1399-0004.1987.tb03313.x. Clin Genet. 1987. PMID: 3677467
Antisense downregulation of mutant huntingtin in a cell model.
Hasholt L, Abell K, Nørremølle A, Nellemann C, Fenger K, Sørensen SA. Hasholt L, et al. Among authors: fenger k. J Gene Med. 2003 Jun;5(6):528-38. doi: 10.1002/jgm.378. J Gene Med. 2003. PMID: 12797118
4p16.3 haplotype modifying age at onset of Huntington disease.
Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L. Nørremølle A, et al. Among authors: fenger k. Clin Genet. 2009 Mar;75(3):244-50. doi: 10.1111/j.1399-0004.2008.01136.x. Clin Genet. 2009. PMID: 19250382
HLA determinants in 70 Danish patients with idiopathic haemochromatosis.
Milman N, Graudal N, Nielsen LS, Fenger K. Milman N, et al. Among authors: fenger k. Clin Genet. 1988 Apr;33(4):286-92. doi: 10.1111/j.1399-0004.1988.tb03450.x. Clin Genet. 1988. PMID: 3359685
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.
Bergthorsson JT, Ejlertsen B, Olsen JH, Borg A, Nielsen KV, Barkardottir RB, Klausen S, Mouridsen HT, Winther K, Fenger K, Niebuhr A, Harboe TL, Niebuhr E. Bergthorsson JT, et al. Among authors: fenger k. J Med Genet. 2001 Jun;38(6):361-8. doi: 10.1136/jmg.38.6.361. J Med Genet. 2001. PMID: 11389159 Free PMC article.
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
Nielsen JE, Koefoed P, Abell K, Hasholt L, Eiberg H, Fenger K, Niebuhr E, Sørensen SA. Nielsen JE, et al. Among authors: fenger k. Hum Mol Genet. 1997 Oct;6(11):1811-6. doi: 10.1093/hmg/6.11.1811. Hum Mol Genet. 1997. PMID: 9302257
A study of psychiatric morbidity in patients with Huntington's disease, their relatives, and controls. Admissions to psychiatric hospitals in Denmark from 1969 to 1991.
Jensen P, Sørensen SA, Fenger K, Bolwig TG. Jensen P, et al. Among authors: fenger k. Br J Psychiatry. 1993 Dec;163:790-7. doi: 10.1192/bjp.163.6.790. Br J Psychiatry. 1993. PMID: 8306121
Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families.
Nørremølle A, Riess O, Epplen JT, Fenger K, Hasholt L, Sørensen SA. Nørremølle A, et al. Among authors: fenger k. Hum Mol Genet. 1993 Sep;2(9):1475-6. doi: 10.1093/hmg/2.9.1475. Hum Mol Genet. 1993. PMID: 8242074
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
Bisgaard ML, Fenger K, Bülow S, Niebuhr E, Mohr J. Bisgaard ML, et al. Among authors: fenger k. Hum Mutat. 1994;3(2):121-5. doi: 10.1002/humu.1380030206. Hum Mutat. 1994. PMID: 8199592
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