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Page 1
[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.
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion.
Lybaek H, Ørstavik KH, Prescott T, Hovland R, Breilid H, Stansberg C, Steen VM, Houge G. Lybaek H, et al. Among authors: houge g. Eur J Hum Genet. 2009 Jul;17(7):904-10. doi: 10.1038/ejhg.2008.261. Epub 2009 Jan 21. Eur J Hum Genet. 2009. PMID: 19156171 Free PMC article.
[Determination of chromosome aberrations with the help of DNA arrays].
Rødningen OK, Prescott TE, Hovland R, Eiklid K, Houge G. Rødningen OK, et al. Among authors: houge g. Tidsskr Nor Laegeforen. 2010 May 6;130(9):944-7. doi: 10.4045/tidsskr.10.0101. Tidsskr Nor Laegeforen. 2010. PMID: 20453958 Free article. Norwegian. No abstract available.
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.
Rainger J, Pehlivan D, Johansson S, Bengani H, Sanchez-Pulido L, Williamson KA, Ture M, Barker H, Rosendahl K, Spranger J, Horn D, Meynert A, Floyd JA, Prescott T, Anderson CA, Rainger JK, Karaca E, Gonzaga-Jauregui C, Jhangiani S, Muzny DM, Seawright A, Soares DC, Kharbanda M, Murday V, Finch A; UK10K; Baylor-Hopkins Center for Mendelian Genomics; Gibbs RA, van Heyningen V, Taylor MS, Yakut T, Knappskog PM, Hurles ME, Ponting CP, Lupski JR, Houge G, FitzPatrick DR. Rainger J, et al. Among authors: houge g. Am J Hum Genet. 2014 Jun 5;94(6):915-23. doi: 10.1016/j.ajhg.2014.05.005. Am J Hum Genet. 2014. PMID: 24906020 Free PMC article.
171 results