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171 results

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Page 1
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB, et al. Karadima G, et al. Among authors: houge g. Eur J Hum Genet. 1998 Sep-Oct;6(5):432-8. doi: 10.1038/sj.ejhg.5200212. Eur J Hum Genet. 1998. PMID: 9801867
[Fetal valproate syndrome].
Houge G, Fiskerstrand T, Øyen N. Houge G, et al. Tidsskr Nor Laegeforen. 2003 Aug 28;123(16):2331. Tidsskr Nor Laegeforen. 2003. PMID: 14508573 Free article. Norwegian. No abstract available.
[More accurate fetal diagnostics].
Sørensen IW, Glad R, Houge G, Blomhoff A, Haug MG, Steen VM. Sørensen IW, et al. Among authors: houge g. Tidsskr Nor Laegeforen. 2021 Oct 7;141(2021-14). doi: 10.4045/tidsskr.21.0424. Print 2021 Oct 12. Tidsskr Nor Laegeforen. 2021. PMID: 34641655 Free article. Norwegian. No abstract available.
A national precision cancer medicine implementation initiative for Norway.
Taskén K, Russnes HEG, Aas E, Bjørge L, Blix ES; CONNECT Public–Private Partnership Consortium; Enerly E, Fagereng GL, Flobak Å, Gilje B, Gjertsen BT, Guren TK, Heix J, Hovig E, Hovland R; InPreD-Norway and National Molecular Tumor Board Consortium; IMPRESS-Norway Consortium; Lønning PE, Meza-Zepeda LA, Mæhle PM, Nilsen HL, Thoresen SØ, Widerberg K, Smeland S, Helland Å. Taskén K, et al. Nat Med. 2022 May;28(5):885-887. doi: 10.1038/s41591-022-01777-4. Nat Med. 2022. PMID: 35513529 No abstract available.
[Ataxia due to vitamin E deficiency].
Gjerde IO, Storstein A, Skeie GO, Wester K, Hegrestad S, Houge G. Gjerde IO, et al. Among authors: houge g. Tidsskr Nor Laegeforen. 1998 Aug 30;118(20):3126-8. Tidsskr Nor Laegeforen. 1998. PMID: 9760855 Norwegian.
Locus conversions are rare in the LRFN5 locus.
Sampson J; Genomics England Research Consortium; Houge G, Banka S. Sampson J, et al. Among authors: houge g. Autism Res. 2023 Jun;16(6):1084-1085. doi: 10.1002/aur.2963. Epub 2023 May 31. Autism Res. 2023. PMID: 37254875 No abstract available.
Absent CNKSR2 causes seizures and intellectual, attention, and language deficits.
Vaags AK, Bowdin S, Smith ML, Gilbert-Dussardier B, Brocke-Holmefjord KS, Sinopoli K, Gilles C, Haaland TB, Vincent-Delorme C, Lagrue E, Harbuz R, Walker S, Marshall CR, Houge G, Kalscheuer VM, Scherer SW, Minassian BA. Vaags AK, et al. Among authors: houge g. Ann Neurol. 2014 Nov;76(5):758-64. doi: 10.1002/ana.24274. Epub 2014 Oct 4. Ann Neurol. 2014. PMID: 25223753
[Volar luxation of the lunate].
Houge G. Houge G. Tidsskr Nor Laegeforen. 1986 Feb 20;106(5):397-9. Tidsskr Nor Laegeforen. 1986. PMID: 3961759 Norwegian. No abstract available.
171 results