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Year | Number of Results |
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2000 | 2 |
2004 | 1 |
2014 | 1 |
2018 | 1 |
2024 | 0 |
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Page 1
Whole-exome sequencing for diagnosis of hereditary ichthyosis.
J Eur Acad Dermatol Venereol. 2018 Jun;32(6):1022-1027. doi: 10.1111/jdv.14870. Epub 2018 Mar 9.
J Eur Acad Dermatol Venereol. 2018.
PMID: 29444371
Application of molecular genetics for diagnosing familial hypercholesterolemia in Norway: results from a family-based screening program.
Leren TP, Manshaus T, Skovholt U, Skodje T, Nossen IE, Teie C, Sørensen S, Bakken KS.
Leren TP, et al. Among authors: skodje t.
Semin Vasc Med. 2004 Feb;4(1):75-85. doi: 10.1055/s-2004-822989.
Semin Vasc Med. 2004.
PMID: 15199436
Review.
Item in Clipboard
Identification of copy number variants from exome sequence data.
Samarakoon PS, Sorte HS, Kristiansen BE, Skodje T, Sheng Y, Tjønnfjord GE, Stadheim B, Stray-Pedersen A, Rødningen OK, Lyle R.
Samarakoon PS, et al. Among authors: skodje t.
BMC Genomics. 2014 Aug 7;15(1):661. doi: 10.1186/1471-2164-15-661.
BMC Genomics. 2014.
PMID: 25102989
Free PMC article.
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[Diagnostic DNA testing for Huntington disease].
Helle JR, Braathen GJ, Skodje T, Berg K.
Helle JR, et al. Among authors: skodje t.
Tidsskr Nor Laegeforen. 2000 Aug 30;120(20):2408-10.
Tidsskr Nor Laegeforen. 2000.
PMID: 11475226
Free article.
Norwegian.
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[Genetic counseling in presymptomatic testing for Huntington disease].
Helle JR, Braathen GJ, Pedersen JC, Skodje T, Stokke B, Berg K.
Helle JR, et al. Among authors: skodje t.
Tidsskr Nor Laegeforen. 2000 Aug 30;120(20):2412-6.
Tidsskr Nor Laegeforen. 2000.
PMID: 11475227
Free article.
Norwegian.
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