Genomic structure and restricted neural expression of the zebrafish wnt-1 (int-1) gene.

Por Molven, A, Njølstad, P R, Fjose, A
Publicado em 1991

The zebrafish homeobox gene hox-2.2: transcription unit, potential regulatory regions and in situ localization of transcripts.

Por Njølstad, P R, Molven, A, Apold, J, Fjose, A
Publicado em 1990

Primary structure, developmentally regulated expression and potential duplication of the zebrafish homeobox gene ZF-21.

Por Njølstad, P R, Molven, A, Hordvik, I, Apold, J, Fjose, A
Publicado em 1988

Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes

Por Bjørnvold, M., Undlien, D. E., Joner, G., Dahl-Jørgensen, K., Njølstad, P. R., Akselsen, H. E., Gervin, K., Rønningen, K. S., Stene, L. C.
Publicado em 2008

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

Por Johnson, D, Horsley, S W, Moloney, D M, Oldridge, M, Twigg, S R, Walsh, S, Barrow, M, Njølstad, P R, Kunz, J, Ashworth, G J, Wall, S A, Kearney, L, Wilkie, A O
Publicado em 1998

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function

Por Lacbawan, F, Solomon, B D, Roessler, E, El-Jaick, K, Domené, S, Vélez, J I, Zhou, N, Hadley, D, Balog, J Z, Long, R, Fryer, A, Smith, W, Omar, S, McLean, S D, Clarkson, K, Lichty, A, Clegg, N J, Delgado, M R, Levey, E, Stashinko, E, Potocki, L, VanAllen, M I, Clayton-Smith, J, Donnai, D, Bianchi, D W, Juliusson, P B, Njølstad, P R, Brunner, H G, Carey, J C, Hehr, U, Müsebeck, J, Wieacker, P F, Postra, A, Hennekam, R C M, van den Boogaard, M-J H, van Haeringen, A, Paulussen, A, Herbergs, J, Schrander-Stumpel, C T R M, Janecke, A R, Chitayat, D, Hahn, J, McDonald-McGinn, D M, Zackai, E H, Dobyns, W B, Muenke, M
Publicado em 2009