Publikationer 1992 2020

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1998

Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals

Mäkelä-Bengs, P., Järvinen, N., Vuopala, K., Suomalainen, A., Ignatius, J., Sipilä, M., Herva, R., Palotie, A. & Peltonen, L., 1998, I : American Journal of Human Genetics. 63, s. 506-516 11 s.

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Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37

Visapaa, I., Fellman, V., Varilo, T., Palotie, A., Raivio, K. O. & Palotie, L., 1998, I : American Journal of Human Genetics. 63, s. 1396-1403 8 s.

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Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13

Pekkarinen, P., Hovatta, I., Hakola, P., Jarvi, O., Kestila, M., Lenkkeri, U., Adolfsson, R., Holmgren, G., Nylander, P. O., Tranebjaerg, L., Terwilliger, J. D., Lonnqvist, J. & Peltonen, L., 1998, I : American Journal of Human Genetics. 62, s. 362-372 11 s.

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Functional conformational changes of endo-1,4-xylanase II from Trichoderma reesei: A molecular dynamics study

Muilu, J., Torronen, A., Perakyla, M. & Rouvinen, J., 1998, I : Proteins: Structure, Function, and Bioinformatics. 31, s. 434-444 11 s.

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1997

Genomic organization of human and mouse genes for vascular endothelial growth factor C

Chilov, D., Kukk, E., Taira, S., Jeltsch, M., Kaukonen, J., Palotie, A., Joukov, V. & Alitalo, K., 1997, I : Journal of Biological Chemistry. 272, s. 25176-25183 8 s.

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Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation

Tyni, T., Rapola, J., Palotie, A. & Pihko, H., 1997, I : Turkish Journal of Pediatrics. 131, s. 766-768 3 s.

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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patients

Tyni, T., Palotie, A., Viinikka, L., Valanne, L., Salo, M. K., vonDobeln, U., Jackson, S., Wanders, R., Venizelos, N. & Pihko, H., 1997, I : Turkish Journal of Pediatrics. 130, s. 67-76 10 s.

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Pathology of long-chain 3-hydroxyacyl-coA dehydrogenase deficiency caused by the G1528C mutation

Tyni, T., Rapola, J., Paetau, A., Palotie, A. & Pihko, H., 1997, I : Fetal and Pediatric Pathology (Print Edition). 17, s. 427-447 21 s.

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The assignment of the lethal congenital contracture syndrome (LCCS) locus to chromosome 9q33-34.

Makela-Bengs, P., Jarvinen, N., Vuopala, K., Suomalainen, A., Palotie, A. & Peltonen, L., 1997, I : American Journal of Human Genetics. 61, s. A30-A30 1 s.

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1996

Ab initio study of small zinc sulfide crystallites

Muilu, J. & Pakkanen, T. A., 1996, I : Surface Science. 364, s. 439-452 14 s.

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1995

Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree

Pekkarinen, P., Terwilliger, J., Bredbacka, P. E., Lönnqvist, J. & Peltonen, L., 1995, I : Genome Research. 5, s. 105-115 11 s.

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THE HUMAN GENE FOR XANTHINE DEHYDROGENASE (XDH) IS LOCALIZED ON CHROMOSOME BAND 2P22

RYTKONEN, E. M. K., HALILA, R., LAAN, M., SAKSELA, M., KALLIONIEMI, O. P., PALOTIE, A. & RAIVIO, K. O., 1995, I : Cytogenetic and Genome Research. 68, s. 61-63 3 s.

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1994

AB-INITIO MODELS FOR ZNS SURFACES - INFLUENCE OF CLUSTER-SIZE ON SURFACE-PROPERTIES

MUILU, J. & PAKKANEN, T. A., 1994, I : Physical Review. B, Condensed Matter. 49, s. 11185-11190 6 s.

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1993

AB-INITIO MOLECULAR-ORBITAL CALCULATIONS ON LARGE LATTICE CLUSTER-MODELS - USE OF TRANSLATIONAL SYMMETRY

PAKKANEN, T. A. & MUILU, J., 1993, I : Theoretical Chemistry Accounts. 86, s. 285-296 12 s.

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1992

MODEL-CALCULATIONS FOR SURFACES AND CHEMISORPTION PROCESSES OF ZINC-CHALCOGENIDE THIN-FILMS BY AN ABINITIO CLUSTER APPROACH

TOTH, K., PAKKANEN, T. A., HIRVA, P. & MUILU, J., 1992, I : Surface Science. 277, s. 395-406 12 s.

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